16-3706759-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706759
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706759
    reference: chr 16
allele count: 1
allele frequency: 1.463528860789135e-5
allele num: 68328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1295C>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+5G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+5G>C
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18599
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.436+5G>C
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

16-3706762-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706762
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706762
    reference: chr 16
allele count: 2
allele frequency: 3.034348828741352e-5
allele num: 65912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1292G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+8C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+8C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18331
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.436+8C>T
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

16-3706769-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706769
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706769
    reference: chr 16
allele count: 1
allele frequency: 1.668947561667613e-5
allele num: 59918
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+15G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1285C>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+15G>C
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-3706770-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706770
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706770
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 59798
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1284C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+16G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21878
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

16-3706773-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706773
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706774
    reference: chr 16
allele count: 1
allele frequency: 1.711859764448096e-5
allele num: 58416
alternate allele: AG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1280dupC
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+22dupG
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+22dupG
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 8876
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21889
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-3706784-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706784
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706784
    reference: chr 16
allele count: 1
allele frequency: 2.244366639734267e-5
allele num: 44556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1270G>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+30C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+30C>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

16-3706784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706784
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706784
    reference: chr 16
allele count: 1
allele frequency: 2.244366639734267e-5
allele num: 44556
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1270G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+30C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+30C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22900
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

16-3706785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706785
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706785
    reference: chr 16
allele count: 3
allele frequency: 6.738544474393532e-5
allele num: 44520
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+31G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1269C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+31G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

16-3706792-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706792
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706792
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 38720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1262G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+38C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+38C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15364
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24527
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-3706793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706793
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706793
    reference: chr 16
allele count: 2
allele frequency: 5.169027189083014e-5
allele num: 38692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1261C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+39G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+39G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24567
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-3706794-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706794
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706794
    reference: chr 16
allele count: 3
allele frequency: 7.885191610156126e-5
allele num: 38046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1260G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+40C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-3706798-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706798
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706798
    reference: chr 16
allele count: 1
allele frequency: 2.690631222084701e-5
allele num: 37166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1256A>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+44T>C
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15610
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

16-3706803-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706803
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706804
    reference: chr 16
allele count: 1
allele frequency: 2.899895603758265e-5
allele num: 34484
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+49_*164+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1250_*76+1251insT
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.183+49_183+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*164+49_*164+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.43+49_43+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.232+49_232+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+49_198+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*164+49_*164+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.436+49_436+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*204+49_*204+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.138+49_138+50insA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.436+49_436+50insA
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25766
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15637
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-3706919-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706919
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706919
    reference: chr 16
allele count: 2
allele frequency: 4.47447313078885e-5
allele num: 44698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-81C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-81C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-46C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-81C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-81C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-81C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-81C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+165C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1135G>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-46C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+165C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-81C>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26257
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10861
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

16-3706925-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706925
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706925
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 45228
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-75A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-75A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-75A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-75A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-75A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+171A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+171A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-75A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-40A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1129T>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-75A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-40A>G
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10595
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

16-3706927-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706927
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706927
    reference: chr 16
allele count: 1
allele frequency: 2.194329851663302e-5
allele num: 45572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-38A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+173A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-73A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-73A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+173A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-73A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-73A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-73A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-73A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1127T>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-38A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-73A>G
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

16-3706928-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706928
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706928
    reference: chr 16
allele count: 3
allele frequency: 6.576351440220966e-5
allele num: 45618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-72T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-72T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-72T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-72T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-37T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-72T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-72T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-37T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+174T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1126A>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-72T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+174T>C
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11003
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10050
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

16-3706930-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706930
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706930
    reference: chr 16
allele count: 1
allele frequency: 2.182834191914782e-5
allele num: 45812
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+176G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-70G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-70G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1124C>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-70G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-35G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-35G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-70G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-70G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-70G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-70G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+176G>C
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

16-3706934-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706934
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706934
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 46468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-66C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-66C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-66C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1120G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+180C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-66C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-66C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-31C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-66C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+180C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-66C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-31C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28215
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

16-3706938-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706938
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706938
    reference: chr 16
allele count: 1
allele frequency: 2.089078298654634e-5
allele num: 47868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-62T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-62T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-62T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-62T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-62T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1116A>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-27T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+184T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-62T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-62T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+184T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-27T>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11040
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29085
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-3706939-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706939
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706939
    reference: chr 16
allele count: 1
allele frequency: 2.080386119663809e-5
allele num: 48068
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-61G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-26G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-61G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+185G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+185G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-61G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-61G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-26G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-61G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1115C>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-61G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-61G>C
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

16-3706942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706942
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706942
    reference: chr 16
allele count: 1
allele frequency: 2.038403522361287e-5
allele num: 49058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-58A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+188A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-58A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-58A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-58A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-23A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-23A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+188A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-58A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-58A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-58A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1112T>C
  variant of: http://identifiers.org/hgnc/16264
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

16-3706945-G-GTGAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706945
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706949
    reference: chr 16
allele count: 9
allele frequency: 1.802306952899712e-4
allele num: 49936
alternate allele: GTGAC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-51_437-48dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-51_*165-48dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+195_198+198dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-16_184-13dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-16_139-13dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1105_*76+1108dupGTCA
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-51_44-48dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-51_*165-48dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-51_*205-48dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+195_*164+198dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-51_233-48dupCTGA
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-51_437-48dupCTGA
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

16-3706949-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706949
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706949
    reference: chr 16
allele count: 1
allele frequency: 1.924853711117955e-5
allele num: 51952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-51C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-51C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-51C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+195C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+195C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-16C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1105G>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-51C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-51C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-16C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-51C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-51C>G
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10798
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-3706956-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706956
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706956
    reference: chr 16
allele count: 8
allele frequency: 1.428826576174317e-4
allele num: 55990
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1098A>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+202T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-9T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+202T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-44T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-9T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-44T>C
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10212
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-3706958-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706958
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706958
    reference: chr 16
allele count: 1
allele frequency: 1.747579602250883e-5
allele num: 57222
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-42C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-42C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+204C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-42C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-42C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-42C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-7C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+204C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-7C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1096G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-42C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-42C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.139-7C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-3706959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706959
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706959
    reference: chr 16
allele count: 2
allele frequency: 3.430649421935573e-5
allele num: 58298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+205C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-41C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+205C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-41C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-41C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1095G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-41C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-41C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-6C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-6C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-41C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-41C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.139-6C>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

16-3706960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706960
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706960
    reference: chr 16
allele count: 2
allele frequency: 3.362135628551256e-5
allele num: 59486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.198+206C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.184-5C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.139-5C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1094G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-40C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*164+206C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28107
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9933
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10292
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.139-5C>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-3706967-AGTGTGCCTCACACGACGTG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706967
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706948
    reference: chr 16
allele count: 1
allele frequency: 1.493205913095416e-5
allele num: 66970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsp: ENSP00000461527.1:p.Val49CysfsTer29
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsp: ENSP00000458959.1:p.Val64CysfsTer29
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val49CysfsTer29
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: AGTGTGCCTCACACGACGTG
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/16-3706978-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706978
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706978
    reference: chr 16
allele count: 1
allele frequency: 1.286140549439243e-5
allele num: 77752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-22C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-22C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-210C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-22C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-22C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-22C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.152C>A
  hgvsp: ENSP00000461527.1:p.His51Gln
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.197C>A
  hgvsp: ENSP00000458959.1:p.His66Gln
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-210C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-22C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-22C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1076G>T
  variant of: http://identifiers.org/hgnc/16264
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His51Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

16-3706980-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706980
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706980
    reference: chr 16
allele count: 77
allele frequency: 9.584266865820264e-4
allele num: 80340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-20C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1074G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-20C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-20C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-20C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.154C>T
  hgvsp: ENSP00000461527.1:p.Thr52Met
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-20C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.199C>T
  hgvsp: ENSP00000458959.1:p.Thr67Met
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-208C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-20C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-208C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-20C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6776
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19487
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20471
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr52Met
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

16-3706980-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706980
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706980
    reference: chr 16
allele count: 3
allele frequency: 3.734129947722181e-5
allele num: 80340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.199C>G
  hgvsp: ENSP00000458959.1:p.Thr67Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-20C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.154C>G
  hgvsp: ENSP00000461527.1:p.Thr52Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1074G>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-20C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-208C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-208C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-20C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-20C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-20C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-20C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-20C>G
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6776
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20471
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr52Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-3706981-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706981
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706981
    reference: chr 16
allele count: 6
allele frequency: 7.210845111047014e-5
allele num: 83208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1073C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.200G>A
  hgvsp: ENST00000570807.1:c.200G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-207G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-19G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-19G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.155G>A
  hgvsp: ENST00000572237.1:c.155G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-19G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-19G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-19G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-207G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-19G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-19G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr52Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

16-3706981-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706981
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706981
    reference: chr 16
allele count: 1
allele frequency: 1.201807518507836e-5
allele num: 83208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-19G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-19G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-19G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-207G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-207G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-19G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-19G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1073C>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.200G>C
  hgvsp: ENST00000570807.1:c.200G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-19G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.155G>C
  hgvsp: ENST00000572237.1:c.155G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-19G>C
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22038
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr52Thr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

16-3706981-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706981
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706981
    reference: chr 16
allele count: 1
allele frequency: 1.201807518507836e-5
allele num: 83208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-19G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-19G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-19G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.200G>T
  hgvsp: ENST00000570807.1:c.200G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.155G>T
  hgvsp: ENST00000572237.1:c.155G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-19G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-19G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-207G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-19G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1073C>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-19G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-207G>T
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr52Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/16-3706983-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706983
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706983
    reference: chr 16
allele count: 9
allele frequency: 1.044640991712515e-4
allele num: 86154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.202C>A
  hgvsp: ENSP00000458959.1:p.Thr68Lys
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-205C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-205C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1071G>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-17C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-17C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.157C>A
  hgvsp: ENSP00000461527.1:p.Thr53Lys
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-17C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-17C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-17C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-17C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-17C>A
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6385
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7458
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23671
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr53Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum

16-3706983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706983
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706983
    reference: chr 16
allele count: 20
allele frequency: 2.321424426027811e-4
allele num: 86154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.157C>T
  hgvsp: ENSP00000461527.1:p.Thr53Met
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-17C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1071G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-17C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-17C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-205C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.202C>T
  hgvsp: ENSP00000458959.1:p.Thr68Met
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-17C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-17C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-17C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-205C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-17C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6385
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23671
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7458
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr53Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

16-3706984-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706984
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706984
    reference: chr 16
allele count: 6
allele frequency: 6.752802413001395e-5
allele num: 88852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.203G>A
  hgvsp: ENST00000570807.1:c.203G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-204G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-204G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.158G>A
  hgvsp: ENST00000572237.1:c.158G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1070C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-16G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-16G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25299
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr53Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-3706984-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706984
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706984
    reference: chr 16
allele count: 1
allele frequency: 1.125467068833566e-5
allele num: 88852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.203G>C
  hgvsp: ENST00000570807.1:c.203G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-204G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.158G>C
  hgvsp: ENST00000572237.1:c.158G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-16G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-16G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1070C>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-16G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-16G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-16G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-16G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-204G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-16G>C
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr53Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-3706985-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706985
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706985
    reference: chr 16
allele count: 1
allele frequency: 1.103192639498709e-5
allele num: 90646
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.159T>C
  hgvsp: ENSP00000461527.1:p.Trp54Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-15T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-15T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-203T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-15T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-15T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-15T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1069A>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-203T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-15T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.204T>C
  hgvsp: ENSP00000458959.1:p.Trp69Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-15T>C
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp54Arg
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-3706986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706986
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706986
    reference: chr 16
allele count: 1
allele frequency: 1.079587165867772e-5
allele num: 92628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-202G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.160G>A
  hgvsp: ENSP00000461527.1:p.Trp54Ter
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-202G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-14G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-14G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.205G>A
  hgvsp: ENSP00000458959.1:p.Trp69Ter
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1068C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-14G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-14G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-14G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-14G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-14G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp54Ter
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-3706988-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706988
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706988
    reference: chr 16
allele count: 1
allele frequency: 1.048240005031552e-5
allele num: 95398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.162C>A
  hgvsp: ENSP00000461527.1:p.Leu55Met
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-12C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-200C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-200C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-12C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1066G>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.207C>A
  hgvsp: ENSP00000458959.1:p.Leu70Met
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-12C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-12C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-12C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-12C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-12C>A
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu55Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

16-3706992-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706992
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706992
    reference: chr 16
allele count: 10
allele frequency: 9.930289368632201e-5
allele num: 100702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1062G>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-8C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-8C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.166C>G
  hgvsp: ENSP00000461527.1:p.Ser56Cys
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.211C>G
  hgvsp: ENSP00000458959.1:p.Ser71Cys
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-8C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-196C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-8C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-8C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-196C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-8C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-8C>G
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9152
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32117
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser71Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

16-3706993-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706993
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706993
    reference: chr 16
allele count: 2
allele frequency: 1.973126023559125e-5
allele num: 101362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.212T>A
  hgvsp: ENST00000570807.1:c.212T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1061A>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-7T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-7T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-7T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.167T>A
  hgvsp: ENST00000572237.1:c.167T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-7T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-195T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-7T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-195T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-7T>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-7T>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9647
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.437-7T>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/16-3706997-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706997
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706997
    reference: chr 16
allele count: 1
allele frequency: 9.483886876197341e-6
allele num: 105442
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-3C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-3C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.216C>A
  hgvsp: ENSP00000458959.1:p.Gln73Lys
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-3C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-3C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-3C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-3C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.171C>A
  hgvsp: ENSP00000461527.1:p.Gln58Lys
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-3C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-191C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-191C>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1057G>T
  variant of: http://identifiers.org/hgnc/16264
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln73Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

16-3706998-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3706998
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3706998
    reference: chr 16
allele count: 1
allele frequency: 9.3905531035778e-6
allele num: 106490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*165-2A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.437-2A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-190A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.172A>G
  hgvsp: ENSP00000461527.1:p.Gln58Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.217A>G
  hgvsp: ENSP00000458959.1:p.Gln73Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.44-2A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.437-2A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*165-2A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-190A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.233-2A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*205-2A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1056T>C
  variant of: http://identifiers.org/hgnc/16264
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.437-2A>G
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

16-3707004-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707004
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707004
    reference: chr 16
allele count: 8
allele frequency: 7.246245539030091e-5
allele num: 110402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-184C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*169C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.441C>G
  hgvsp: ENST00000246949.5:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.178C>G
  hgvsp: ENSP00000461527.1:p.Ser60Ter
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*169C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1050G>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.48C>G
  hgvsp: ENST00000570664.1:c.48C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.237C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.223C>G
  hgvsp: ENSP00000458959.1:p.Ser75Ter
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.441C>G
  hgvsp: ENST00000407479.1:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*209C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-184C>G
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36881
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser75Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

16-3707007-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707007
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707007
    reference: chr 16
allele count: 1
allele frequency: 8.927455496634349e-6
allele num: 112014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*212G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.226G>T
  hgvsp: ENSP00000458959.1:p.Gly76Val
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.240G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.444G>T
  hgvsp: ENSP00000246949.5:p.Arg148Ser
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.181G>T
  hgvsp: ENSP00000461527.1:p.Gly61Val
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1047C>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.51G>T
  hgvsp: ENSP00000459507.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-181G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-181G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.444G>T
  hgvsp: ENSP00000385905.1:p.Arg148Ser
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*172G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*172G>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg148Ser
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

16-3707010-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707010
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707011
    reference: chr 16
allele count: 1
allele frequency: 8.843609607697478e-6
allele num: 113076
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-175dupT
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.450dupT
  hgvsp: ENSP00000246949.5:p.Ala151CysfsTer21
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*178dupT
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*218dupT
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.232dupT
  hgvsp: ENSP00000458959.1:p.Leu78PhefsTer134
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1043dupA
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.450dupT
  hgvsp: ENSP00000385905.1:p.Ala151CysfsTer21
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.246dupT
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.57dupT
  hgvsp: ENSP00000459507.1:p.Ala20CysfsTer21
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-175dupT
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*178dupT
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.187dupT
  hgvsp: ENSP00000461527.1:p.Leu63PhefsTer61
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala151CysfsTer21
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

16-3707018-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707018
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707018
    reference: chr 16
allele count: 1
allele frequency: 8.655610566769381e-6
allele num: 115532
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.192T>C
  hgvsp: ENST00000572237.1:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.251T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1036A>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.455T>C
  hgvsp: ENSP00000385905.1:p.Ile152Thr
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-170T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*183T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.62T>C
  hgvsp: ENSP00000459507.1:p.Ile21Thr
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.455T>C
  hgvsp: ENSP00000246949.5:p.Ile152Thr
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*223T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.237T>C
  hgvsp: ENST00000570807.1:c.237T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-170T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*183T>C
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile152Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

16-3707023-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707023
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707023
    reference: chr 16
allele count: 685
allele frequency: 5.881645830471218e-3
allele num: 116464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.242C>G
  hgvsp: ENSP00000458959.1:p.Phe81Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*188C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1031G>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*188C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-165C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.460C>G
  hgvsp: ENSP00000385905.1:p.Pro154Ala
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-165C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.197C>G
  hgvsp: ENSP00000461527.1:p.Phe66Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*228C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.67C>G
  hgvsp: ENSP00000459507.1:p.Pro23Ala
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.256C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.460C>G
  hgvsp: ENSP00000246949.5:p.Pro154Ala
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38465
  bin: 2.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 12657
  bin: 2.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 3.25e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 128
genotype quality: GenotypeQuality
hgvs: p.Pro154Ala
num of homozygotes: 17
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

16-3707025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707025
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707025
    reference: chr 16
allele count: 7
allele frequency: 5.987921506903218e-5
allele num: 116902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.462C>T
  hgvsp: ENST00000407479.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.199C>T
  hgvsp: ENSP00000461527.1:p.Pro67Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.258C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1029G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*230C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-163C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*190C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.69C>T
  hgvsp: ENST00000570664.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.462C>T
  hgvsp: ENST00000246949.5:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.244C>T
  hgvsp: ENSP00000458959.1:p.Pro82Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*190C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-163C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro82Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-3707030-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707030
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707030
    reference: chr 16
allele count: 2
allele frequency: 1.697908177125781e-5
allele num: 117792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.249A>T
  hgvsp: ENSP00000458959.1:p.Met84Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.467A>T
  hgvsp: ENSP00000246949.5:p.His156Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.74A>T
  hgvsp: ENSP00000459507.1:p.His25Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1024T>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.204A>T
  hgvsp: ENSP00000461527.1:p.Met69Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*195A>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-158A>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*195A>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.467A>T
  hgvsp: ENSP00000385905.1:p.His156Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*235A>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-158A>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.263A>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His156Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-3707031-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707031
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707031
    reference: chr 16
allele count: 1
allele frequency: 8.479031355457952e-6
allele num: 117938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-157T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.264T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*196T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*236T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1023A>G
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-157T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.205T>C
  hgvsp: ENSP00000461527.1:p.Met69Thr
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.468T>C
  hgvsp: ENST00000246949.5:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.468T>C
  hgvsp: ENST00000407479.1:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*196T>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.250T>C
  hgvsp: ENSP00000458959.1:p.Met84Thr
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.75T>C
  hgvsp: ENST00000570664.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met84Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

16-3707033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707033
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707033
    reference: chr 16
allele count: 6
allele frequency: 5.081128688052573e-5
allele num: 118084
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.470C>T
  hgvsp: ENSP00000246949.5:p.Ala157Val
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1021G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*198C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.77C>T
  hgvsp: ENSP00000459507.1:p.Ala26Val
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.252C>T
  hgvsp: ENSP00000458959.1:p.Arg85Trp
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-155C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*238C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*198C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.207C>T
  hgvsp: ENSP00000461527.1:p.Arg70Trp
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.266C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.470C>T
  hgvsp: ENSP00000385905.1:p.Ala157Val
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-155C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38539
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala157Val
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

16-3707034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707034
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707034
    reference: chr 16
allele count: 2
allele frequency: 1.688533171234149e-5
allele num: 118446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-154G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*199G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.253G>A
  hgvsp: ENSP00000458959.1:p.Arg85Gln
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.471G>A
  hgvsp: ENST00000246949.5:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.267G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1020C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.78G>A
  hgvsp: ENST00000570664.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*199G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.471G>A
  hgvsp: ENST00000407479.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.208G>A
  hgvsp: ENSP00000461527.1:p.Arg70Gln
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-154G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*239G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg85Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

16-3707038-C-CCTGCATG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707038
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707045
    reference: chr 16
allele count: 4
allele frequency: 3.365190469780589e-5
allele num: 118864
alternate allele: CCTGCATG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.258_259insTGCATGC
  hgvsp: ENSP00000458959.1:p.Arg87LeufsTer127
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*244_*245insTGCATGC
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.272_273insTGCATGC
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*204_*205insTGCATGC
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.476_477insTGCATGC
  hgvsp: ENSP00000385905.1:p.Gly160AlafsTer14
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.213_214insTGCATGC
  hgvsp: ENSP00000461527.1:p.Arg72LeufsTer54
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*204_*205insTGCATGC
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.83_84insTGCATGC
  hgvsp: ENSP00000459507.1:p.Gly29AlafsTer14
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.476_477insTGCATGC
  hgvsp: ENSP00000246949.5:p.Gly160AlafsTer14
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13963
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly160AlafsTer14
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

16-3707039-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707039
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707039
    reference: chr 16
allele count: 3
allele frequency: 2.524784972479844e-5
allele num: 118822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-149C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.476C>G
  hgvsp: ENSP00000246949.5:p.Pro159Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.258C>G
  hgvsp: ENSP00000458959.1:p.Arg87Gly
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.272C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-149C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.476C>G
  hgvsp: ENSP00000385905.1:p.Pro159Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.83C>G
  hgvsp: ENSP00000459507.1:p.Pro28Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.213C>G
  hgvsp: ENSP00000461527.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1015G>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*244C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*204C>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*204C>G
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro159Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

16-3707039-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707039
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707039
    reference: chr 16
allele count: 1
allele frequency: 8.415949908266146e-6
allele num: 118822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.83C>T
  hgvsp: ENSP00000459507.1:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.258C>T
  hgvsp: ENSP00000458959.1:p.Arg87Trp
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.476C>T
  hgvsp: ENSP00000385905.1:p.Pro159Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-149C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.272C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*244C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*204C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.476C>T
  hgvsp: ENSP00000246949.5:p.Pro159Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*204C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.213C>T
  hgvsp: ENSP00000461527.1:p.Arg72Trp
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-149C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1015G>A
  variant of: http://identifiers.org/hgnc/16264
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro159Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

16-3707042-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707042
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707042
    reference: chr 16
allele count: 3
allele frequency: 2.512604901254627e-5
allele num: 119398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-146G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*207G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-146G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*247G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.479G>A
  hgvsp: ENSP00000385905.1:p.Gly160Glu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1012C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.86G>A
  hgvsp: ENSP00000459507.1:p.Gly29Glu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.479G>A
  hgvsp: ENSP00000246949.5:p.Gly160Glu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.275G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.261G>A
  hgvsp: ENSP00000458959.1:p.Gly88Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.216G>A
  hgvsp: ENSP00000461527.1:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*207G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly160Glu
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

16-3707045-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707045
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707045
    reference: chr 16
allele count: 1
allele frequency: 8.367920739054759e-6
allele num: 119504
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.219A>G
  hgvsp: ENSP00000461527.1:p.Thr74Ala
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1009T>C
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.278A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*210A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*250A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.264A>G
  hgvsp: ENSP00000458959.1:p.Thr89Ala
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.482A>G
  hgvsp: ENSP00000385905.1:p.Asp161Gly
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.89A>G
  hgvsp: ENSP00000459507.1:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-143A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-143A>G
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.482A>G
  hgvsp: ENSP00000246949.5:p.Asp161Gly
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*210A>G
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp161Gly
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: A
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

16-3707046-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707046
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707046
    reference: chr 16
allele count: 7
allele frequency: 5.853625903130854e-5
allele num: 119584
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.483C>T
  hgvsp: ENST00000246949.5:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.220C>T
  hgvsp: ENSP00000461527.1:p.Thr74Met
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.279C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-142C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*211C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.90C>T
  hgvsp: ENST00000570664.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*211C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.265C>T
  hgvsp: ENSP00000458959.1:p.Thr89Met
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1008G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.483C>T
  hgvsp: ENST00000407479.1:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-142C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*251C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14464
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr89Met
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

16-3707047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707047
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707047
    reference: chr 16
allele count: 1
allele frequency: 8.35812911637859e-6
allele num: 119644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.484G>A
  hgvsp: ENSP00000385905.1:p.Ala162Thr
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1007C>T
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-141G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.484G>A
  hgvsp: ENSP00000246949.5:p.Ala162Thr
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-141G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461725
  ensembl transcript: ENST00000570376
  gene symbol: DNASE1
  hgvsc: ENST00000570376.1:c.*212G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.266G>A
  hgvsp: ENST00000570807.1:c.266G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*212G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.91G>A
  hgvsp: ENSP00000459507.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.280G>A
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.221G>A
  hgvsp: ENST00000572237.1:c.221G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*252G>A
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala162Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

16-3707050-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707050
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707050
    reference: chr 16
allele count: 6
allele frequency: 5.106296063045736e-5
allele num: 117502
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-138G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.94G>C
  hgvsp: ENSP00000459507.1:p.Val32Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.283G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.269G>C
  hgvsp: ENSP00000458959.1:p.Gln90His
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-138G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.487G>C
  hgvsp: ENSP00000246949.5:p.Val163Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.224G>C
  hgvsp: ENSP00000461527.1:p.Gln75His
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.487G>C
  hgvsp: ENSP00000385905.1:p.Val163Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*255G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*215G>C
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1004C>G
  variant of: http://identifiers.org/hgnc/16264
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37613
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val163Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD

16-3707050-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707050
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707050
    reference: chr 16
allele count: 250
allele frequency: 2.12762335960239e-3
allele num: 117502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.487G>T
  hgvsp: ENSP00000385905.1:p.Val163Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.283G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*215G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.224G>T
  hgvsp: ENSP00000461527.1:p.Gln75His
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.269G>T
  hgvsp: ENSP00000458959.1:p.Gln90His
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-138G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*255G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1004C>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-138G>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.487G>T
  hgvsp: ENSP00000246949.5:p.Val163Leu
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.94G>T
  hgvsp: ENSP00000459507.1:p.Val32Leu
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 37613
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 3.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 14227
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
hgvs: p.Val163Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-3707054-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707054
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707054
    reference: chr 16
allele count: 3
allele frequency: 2.4942631946523e-5
allele num: 120276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.491C>T
  hgvsp: ENSP00000385905.1:p.Ala164Val
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.287C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.491C>T
  hgvsp: ENSP00000246949.5:p.Ala164Val
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-134C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.98C>T
  hgvsp: ENSP00000459507.1:p.Ala33Val
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-134C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.*1C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*259C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+1000G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*219C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.*1C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15016
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala164Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

16-3707055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3707055
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3707055
    reference: chr 16
allele count: 1
allele frequency: 8.312690152787244e-6
allele num: 120298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458959
  ensembl transcript: ENST00000570807
  gene symbol: DNASE1
  hgvsc: ENST00000570807.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461745
  ensembl transcript: ENST00000576050
  gene symbol: DNASE1
  hgvsc: ENST00000576050.1:c.*220C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000416699
  ensembl transcript: ENST00000414110
  gene symbol: DNASE1
  hgvsc: ENST00000414110.2:c.199-133C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000461527
  ensembl transcript: ENST00000572237
  gene symbol: DNASE1
  hgvsc: ENST00000572237.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000246949
  ensembl transcript: ENST00000246949
  gene symbol: DNASE1
  hgvsc: ENST00000246949.5:c.492C>T
  hgvsp: ENST00000246949.5:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459507
  ensembl transcript: ENST00000570664
  gene symbol: DNASE1
  hgvsc: ENST00000570664.1:c.99C>T
  hgvsp: ENST00000570664.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000385905
  ensembl transcript: ENST00000407479
  gene symbol: DNASE1
  hgvsc: ENST00000407479.1:c.492C>T
  hgvsp: ENST00000407479.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000458467
  ensembl transcript: ENST00000570769
  gene symbol: DNASE1
  hgvsc: ENST00000570769.1:c.*260C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000126602
  ensembl protein: ENSP00000459385
  ensembl transcript: ENST00000575707
  gene symbol: TRAP1
  hgvsc: ENST00000575707.1:c.*76+999G>A
  variant of: http://identifiers.org/hgnc/16264
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000213918
  ensembl transcript: ENST00000573804
  gene symbol: DNASE1
  hgvsc: ENST00000573804.1:n.288C>T
  variant of: http://identifiers.org/hgnc/2956
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000213918
  ensembl protein: ENSP00000459850
  ensembl transcript: ENST00000571460
  gene symbol: DNASE1
  hgvsc: ENST00000571460.1:c.*165-133C>T
  variant of: http://identifiers.org/hgnc/2956
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala164Ala
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 2487
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2104
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 342
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4868
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5360
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6119
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3247
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32025
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5942
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.701972439881113e-5
allele num: 37010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.31e-1

FS
type: SiteQuality
SIO_000300: 1.502e0

DP
type: SiteQuality
SIO_000300: 1.142971e6

MQ
type: SiteQuality
SIO_000300: 5.682e1

QD
type: SiteQuality
SIO_000300: 1.427e1

VQSLOD
type: SiteQuality
SIO_000300: -1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 784
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 342
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6229
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 199
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2364
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6119
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 279
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35624
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.46860908775581e-4
allele num: 5766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3994
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.397e1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.98e-1

FS
type: SiteQuality
SIO_000300: 4.034e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 1.125614e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeDepth
all individuals: 342
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1805
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29392
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8861
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6119
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 353
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.11604138102954e-5
allele num: 32092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.79e-1

MQ
type: SiteQuality
SIO_000300: 5.777e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

DP
type: SiteQuality
SIO_000300: 1.08473e6

QD
type: SiteQuality
SIO_000300: 5.94e0

GenotypeDepth
all individuals: 2560
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1798
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2104
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29875
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8908
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3339
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 350
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6118
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

VQSLOD
type: SiteQuality
SIO_000300: -1.531e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

FS
type: SiteQuality
SIO_000300: 4.26e0

DP
type: SiteQuality
SIO_000300: 1.083697e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e0

QD
type: SiteQuality
SIO_000300: 1.099e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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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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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.25e1
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GenotypeQuality
all individuals: 350
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.211510052026463e-5
allele num: 31138
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3278
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3086
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
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.772e0

VQSLOD
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MQRankSum
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SIO_000300: -2.72e-1

ReadPosRankSum
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DP
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SIO_000300: 1.072343e6

InbreedingCoeff
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SIO_000300: -1.91e-2

BaseQRankSum
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SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 6.017e1

QD
type: SiteQuality
SIO_000300: 6.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4180
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1956
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.563791874554526e-4
allele num: 2806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23046
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

QD
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 7.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1956
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23046
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.031140441328109e-4
allele num: 9698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 7.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.96145e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.57e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

QD
type: SiteQuality
SIO_000300: 1.208e1

GenotypeDepth
all individuals: 437
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 289
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GenotypeQuality
all individuals: 342
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.076142131979696e-4
allele num: 1970
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.347070074769605e-5
allele num: 23004
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.032417922775139e-4
allele num: 9686
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.253e1

ReadPosRankSum
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ClippingRankSum
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SIO_000300: 1.37e0

MQRankSum
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BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -2.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.98e-2

DP
type: SiteQuality
SIO_000300: 9.94488e5

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1975
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2120
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2148
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1538
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 19484
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.101e0

InbreedingCoeff
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QD
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MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.63251e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19444
num of homozygotes: 0

South Asian
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
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African
type: Population
allele count: 1
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allele num: 3804
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 6.46830530401035e-4
allele num: 1546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.35e-2

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.787e1

ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.671e0

BaseQRankSum
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SIO_000300: -1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 198
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

East 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: 1988
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 5.324813631522897e-4
allele num: 3756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19050
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European (Finnish)
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allele count: 0
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South Asian
type: Population
allele count: 1
allele frequency: 1.07828337287039e-4
allele num: 9274
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.33e-2

MQ
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 5.397819281010472e-5
allele num: 18526
num of homozygotes: 0

South Asian
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African
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European (Finnish)
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Other
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East Asian
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Latino
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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Latino
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Other
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FS
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 2476
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African
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South Asian
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Latino
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European (Non-Finnish)
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Other
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European (Finnish)
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ReadPosRankSum
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InbreedingCoeff
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DP
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FS
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MQRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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MQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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QD
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DP
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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Other
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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QD
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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East Asian
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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DP
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MQRankSum
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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Other
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European (Non-Finnish)
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African
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East Asian
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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QD
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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African
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Latino
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allele num: 2330
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European (Finnish)
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South Asian
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East Asian
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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Other
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African
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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VQSLOD
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MQRankSum
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DP
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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South Asian
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Latino
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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European (Finnish)
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VQSLOD
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QD
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ClippingRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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QD
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MQ
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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African
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Other
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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Latino
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European (Non-Finnish)
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African
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allele num: 5702
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European (Finnish)
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allele frequency: 0.0e0
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Other
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QD
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VQSLOD
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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East Asian
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

Latino
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allele frequency: 1.643655489809336e-4
allele num: 6084
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 4.476876930653176e-5
allele num: 44674
num of homozygotes: 0

MQ
type: SiteQuality
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FS
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SIO_000300: 0.0e0

VQSLOD
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ReadPosRankSum
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DP
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QD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.18e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

South Asian
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allele frequency: 1.531393568147014e-4
allele num: 13060
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 1.540832049306626e-4
allele num: 6490
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 6.469142191745374e-5
allele num: 46374
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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DP
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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QD
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FS
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5800
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13060
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.156380730581792e-5
allele num: 46374
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3440
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5800
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.156380730581792e-5
allele num: 46374
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7384
num of homozygotes: 0

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

Other
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allele count: 0
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

QD
type: SiteQuality
SIO_000300: 1.335e1

ClippingRankSum
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SIO_000300: 2.11e-1

FS
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SIO_000300: 1.1251e1

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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MQ
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VQSLOD
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SIO_000300: -3.25e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 6
allele frequency: 1.248023962060072e-4
allele num: 48076
num of homozygotes: 0

South Asian
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allele frequency: 1.510117789187557e-4
allele num: 13244
num of homozygotes: 0

African
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allele count: 1
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allele num: 7600
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.080039936766786e-5
allele num: 48076
num of homozygotes: 0

South Asian
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allele frequency: 7.550588945937783e-5
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num of homozygotes: 0

Latino
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allele frequency: 2.317497103128621e-3
allele num: 6904
num of homozygotes: 0

European (Finnish)
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allele count: 0
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African
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allele count: 2
allele frequency: 2.631578947368421e-4
allele num: 7600
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Other
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
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num of homozygotes: 0

South Asian
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allele num: 13484
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East Asian
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European (Finnish)
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Latino
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Other
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African
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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African
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South Asian
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East Asian
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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Other
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East Asian
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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East Asian
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South Asian
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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Other
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BaseQRankSum
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FS
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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African
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Other
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South Asian
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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African
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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Latino
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African
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South Asian
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.284356537374775e-4
allele num: 7786
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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Other
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ClippingRankSum
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BaseQRankSum
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QD
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MQRankSum
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

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

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

South Asian
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allele frequency: 5.204267499349467e-4
allele num: 15372
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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DP
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.608441098886959e-5
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15680
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62696
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 9.204712812960235e-5
allele num: 10864
num of homozygotes: 0

Other
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allele count: 0
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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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.48e0

InbreedingCoeff
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ClippingRankSum
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QD
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FS
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MQ
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11126
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63904
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European (Finnish)
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East Asian
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African
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South Asian
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allele num: 15960
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Other
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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QD
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 838
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South Asian
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African
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allele frequency: 5.055611729019212e-4
allele num: 9890
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European (Finnish)
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European (Non-Finnish)
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allele count: 11
allele frequency: 1.709029892486483e-4
allele num: 64364
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Latino
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East Asian
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QD
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 2.667615152054063e-4
allele num: 11246
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.832361773538245e-5
allele num: 11322
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5764
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10000
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.537988311288834e-5
allele num: 65020
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -8.97e-1

VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.337e1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.982032341784787e-5
allele num: 10018
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65070
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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MQRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5850
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 1
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allele num: 854
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South Asian
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allele count: 1
allele frequency: 6.129704548240775e-5
allele num: 16314
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.143072150382407e-5
allele num: 65114
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ClippingRankSum
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SIO_000300: -8.699999999999999e-2

BaseQRankSum
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VQSLOD
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MQRankSum
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QD
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DP
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InbreedingCoeff
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SIO_000300: 1.41e-2

FS
type: SiteQuality
SIO_000300: 5.952e0

ReadPosRankSum
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SIO_000300: 4.25e-1

MQ
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SIO_000300: 5.948e1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65284
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

South Asian
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allele count: 1
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allele num: 16356
num of homozygotes: 0

Other
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
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num of homozygotes: 0

African
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allele count: 0
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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BaseQRankSum
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SIO_000300: -8.53e-1

ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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SIO_000300: 5.433e0

QD
type: SiteQuality
SIO_000300: 8.859999999999999e0

DP
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SIO_000300: 1.434131e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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African
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Latino
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allele frequency: 3.506311360448808e-4
allele num: 11408
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DP
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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Other
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African
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allele frequency: 1.981375074301565e-4
allele num: 10094
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65474
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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East Asian
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Other
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European (Non-Finnish)
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ClippingRankSum
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SIO_000300: -1.58e-1

QD
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SIO_000300: 7.67e0

VQSLOD
type: SiteQuality
SIO_000300: -1.475e0

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
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SIO_000300: -2.555e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.54e-1

FS
type: SiteQuality
SIO_000300: 1.4323e1

MQ
type: SiteQuality
SIO_000300: 5.915e1

DP
type: SiteQuality
SIO_000300: 1.444739e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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: 2.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5969
bin: 6.75e1
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GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.825483753194597e-4
allele num: 16434
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 3.497e0

DP
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SIO_000300: 1.449494e6

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 8.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.451236e6

ReadPosRankSum
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SIO_000300: -1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.548e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.83e-1

FS
type: SiteQuality
SIO_000300: 8.042e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 23
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GenotypeQuality
all individuals: 277
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variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.946954813359528e-4
allele num: 10180
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.081245439065921e-5
allele num: 16444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.037943919555245e-5
allele num: 65834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.616553507921112e-4
allele num: 6186
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

BaseQRankSum
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SIO_000300: -7.67e-1

DP
type: SiteQuality
SIO_000300: 1.452056e6

FS
type: SiteQuality
SIO_000300: 5.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518187890933382e-5
allele num: 65868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6204
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.45385e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 2.886e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64500
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

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

Latino
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allele count: 6
allele frequency: 5.258545135845749e-4
allele num: 11410
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8574
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5906
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African
type: Population
allele count: 0
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DP
type: SiteQuality
SIO_000300: 1.507034e6

BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.902e1

VQSLOD
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SIO_000300: -2.287e2

FS
type: SiteQuality
SIO_000300: 2.21955e2

QD
type: SiteQuality
SIO_000300: 7.8e-1

GenotypeDepth
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variant carriers: 19

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 77

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

European (Finnish)
type: Population
allele count: 25
allele frequency: 4.232983406705046e-3
allele num: 5906
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.5056967572305e-4
allele num: 11410
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.332633543270352e-4
allele num: 8574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 162
allele frequency: 2.511627906976744e-3
allele num: 64500
num of homozygotes: 0

African
type: Population
allele count: 56
allele frequency: 5.698005698005698e-3
allele num: 9828
num of homozygotes: 0

Other
type: Population
allele count: 1
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allele num: 830
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MQRankSum
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SIO_000300: -9.6e-2

DP
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 2.21955e2

MQ
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InbreedingCoeff
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QD
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VQSLOD
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SIO_000300: -2.287e2

BaseQRankSum
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SIO_000300: -3.344e0

ClippingRankSum
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SIO_000300: 2.28e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 199
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GenotypeQuality
all individuals: 272
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.533502584096473e-5
allele num: 66174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.480525e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

QD
type: SiteQuality
SIO_000300: 1.106e1

FS
type: SiteQuality
SIO_000300: 2.694e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.33e0

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47450
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 920
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6128
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0