16-70395423-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395423
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395423
    reference: chr 16
allele count: 1
allele frequency: 8.269520202437855e-6
allele num: 120926
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+10C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3497C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-3023C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4565C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*6C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+10C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+10C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+10C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4565C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+10C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4075
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

16-70395425-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395425
    reference: chr 16
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*8G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-3021G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+12G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4563G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+12G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4563G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+12G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+12G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3495G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+12G>C
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3078
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-70395428-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395428
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395428
    reference: chr 16
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*11G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+15G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3492G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4560G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+15G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-3018G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+15G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+15G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+15G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4560G>A
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-70395433-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395433
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395433
    reference: chr 16
allele count: 15
allele frequency: 1.244482792951249e-4
allele num: 120532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+20G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-3013G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+20G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*16G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+20G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+20G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4555G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+20G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4555G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3487G>A
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24327
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-70395441-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395441
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395441
    reference: chr 16
allele count: 1
allele frequency: 8.310755780130645e-6
allele num: 120326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+28C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*24C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+28C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+28C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3479C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4547C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+28C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4547C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-3005C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+28C>A
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12767
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

16-70395443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395443
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395443
    reference: chr 16
allele count: 1
allele frequency: 8.321129010784183e-6
allele num: 120176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+30C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+30C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+30C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+30C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4545C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-3003C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4545C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+30C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3477C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*26C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8781
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-70395454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395454
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395454
    reference: chr 16
allele count: 1
allele frequency: 8.351288603831571e-6
allele num: 119742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-2992G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4534G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+41G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+41G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+41G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+41G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+41G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4534G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3466G>A
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7632
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

16-70395459-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395459
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395459
    reference: chr 16
allele count: 8
allele frequency: 6.703536115300821e-5
allele num: 119340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+46A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+46A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+46A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*42A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-2987A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+46A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4529A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+46A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4529A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3461A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11050
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13290
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD

16-70395463-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70395463
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70395463
    reference: chr 16
allele count: 2
allele frequency: 1.682340472064736e-5
allele num: 118882
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.116+50T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*13+50T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.139+50T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*46T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-2983T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-4525T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*174+50T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-4525T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.386+50T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-3457T>C
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12323
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12726
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1873
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

16-70398397-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398397
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398398
    reference: chr 16
allele count: 4
allele frequency: 3.320549218840796e-5
allele num: 120462
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.117-48dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1195dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*175-48dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*123-48dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-522dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1590dupA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-48dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.365dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.140-48dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*14-48dupA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1590dupA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.387-48dupA
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17561
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11232
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

16-70398402-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398402
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398402
    reference: chr 16
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*123-44A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.387-44A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*14-44A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-518A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-44A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1586A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.369A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.117-44A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1586A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1199A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*175-44A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.140-44A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-70398407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398407
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398407
    reference: chr 16
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1581C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1204C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.117-39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*175-39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.140-39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.374C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*123-39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-513C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.387-39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1581C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*14-39C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-70398408-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398408
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398408
    reference: chr 16
allele count: 2
allele frequency: 1.658429798666623e-5
allele num: 120596
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-512A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1580A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-38A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.375A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*14-38A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1205A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1580A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.117-38A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*123-38A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.140-38A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.387-38A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*175-38A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11557
  bin: 3.25e1
  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: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-70398412-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398412
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398412
    reference: chr 16
allele count: 10
allele frequency: 8.286102548805144e-5
allele num: 120684
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.387-34A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.379A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-508A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.140-34A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1576A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*123-34A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-34A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*175-34A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.117-34A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1576A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1209A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*14-34A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18768
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-70398429-GTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398429
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398426
    reference: chr 16
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.387-13_387-11delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*123-13_*123-11delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1555_608-1553delTTC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*14-13_*14-11delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.400_402delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1555_*319-1553delTTC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-13_294-11delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1230_1232delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.117-13_117-11delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.140-13_140-11delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-487_354-485delTTC
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*175-13_*175-11delTTC
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: GTTC
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

16-70398432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398432
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398432
    reference: chr 16
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.387-14C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*14-14C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1229C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.399C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*123-14C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*175-14C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.294-14C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.140-14C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1556C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.117-14C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1556C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-488C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/16-70398451-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398451
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398451
    reference: chr 16
allele count: 4
allele frequency: 3.297174321606383e-5
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1537A>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*128A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*180A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.122A>C
  hgvsp: ENSP00000399208.2:p.Gln41Pro
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.392A>C
  hgvsp: ENSP00000306117.7:p.Gln131Pro
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-469A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1248A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.6A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*19A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.299A>C
  hgvsp: ENSP00000410243.2:p.Gln100Pro
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.145A>C
  hgvsp: ENSP00000460180.1:p.Gln49Pro
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.418A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1537A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln131Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

16-70398489-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398489
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398489
    reference: chr 16
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.337A>T
  hgvsp: ENSP00000410243.2:p.Thr113Ser
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1499A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.160A>T
  hgvsp: ENSP00000399208.2:p.Thr54Ser
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.430A>T
  hgvsp: ENSP00000306117.7:p.Thr144Ser
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.183A>T
  hgvsp: ENSP00000460180.1:p.Thr62Ser
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1499A>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*218A>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1286A>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.456A>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-431A>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*166A>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*57A>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.44A>T
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr144Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

16-70398493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398493
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398493
    reference: chr 16
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1495C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.434C>T
  hgvsp: ENSP00000306117.7:p.Ala145Val
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*61C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1290C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*222C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.460C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.164C>T
  hgvsp: ENSP00000399208.2:p.Ala55Val
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-427C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.187C>T
  hgvsp: ENSP00000460180.1:p.Ala63Val
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.341C>T
  hgvsp: ENSP00000410243.2:p.Ala114Val
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*170C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1495C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19880
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala145Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

16-70398497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398497
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398497
    reference: chr 16
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.191C>T
  hgvsp: ENST00000575878.1:c.191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*226C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.168C>T
  hgvsp: ENST00000443119.2:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1491C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*65C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.438C>T
  hgvsp: ENST00000302243.7:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1294C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.345C>T
  hgvsp: ENST00000417604.2:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1491C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.464C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.52C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-423C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*174C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala146Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-70398513-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398513
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398513
    reference: chr 16
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1310C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.480C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.184C>T
  hgvsp: ENSP00000399208.2:p.Leu62Phe
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1475C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.361C>T
  hgvsp: ENSP00000410243.2:p.Leu121Phe
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*242C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.454C>T
  hgvsp: ENSP00000306117.7:p.Leu152Phe
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.207C>T
  hgvsp: ENSP00000460180.1:p.Leu70Phe
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.68C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1475C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-407C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*190C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu152Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

16-70398528-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398528
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398528
    reference: chr 16
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.83C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.495C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1325C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1460C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.469C>G
  hgvsp: ENSP00000306117.7:p.Pro157Ala
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.222C>G
  hgvsp: ENSP00000460180.1:p.Pro75Ala
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*96C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-392C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*257C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.376C>G
  hgvsp: ENSP00000410243.2:p.Pro126Ala
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1460C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.199C>G
  hgvsp: ENSP00000399208.2:p.Pro67Ala
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*205C>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11870
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro157Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

16-70398531-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398531
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398531
    reference: chr 16
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.472T>A
  hgvsp: ENSP00000306117.7:p.Ser158Thr
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*208T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-389T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.498T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1457T>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.225T>A
  hgvsp: ENSP00000460180.1:p.Ser76Thr
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*99T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*260T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.202T>A
  hgvsp: ENSP00000399208.2:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.379T>A
  hgvsp: ENSP00000410243.2:p.Ser127Thr
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.86T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1328T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1457T>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser158Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

16-70398533-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398533
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398533
    reference: chr 16
allele count: 509
allele frequency: 4.195931018564316e-3
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-387A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1455A>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*262A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.88A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.474A>G
  hgvsp: ENST00000302243.7:c.474A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.381A>G
  hgvsp: ENST00000417604.2:c.381A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.500A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1455A>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*210A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.204A>G
  hgvsp: ENST00000443119.2:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.227A>G
  hgvsp: ENST00000575878.1:c.227A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*101A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1330A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 19758
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11765
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 75
genotype quality: GenotypeQuality
hgvs: p.Ser158Ser
num of homozygotes: 5
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

16-70398536-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398536
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398536
    reference: chr 16
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*213C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1333C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.384C>G
  hgvsp: ENSP00000410243.2:p.Asp128Glu
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.207C>G
  hgvsp: ENSP00000399208.2:p.Asp69Glu
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1452C>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1452C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.230C>G
  hgvsp: ENSP00000460180.1:p.Asp77Glu
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-384C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.503C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.477C>G
  hgvsp: ENSP00000306117.7:p.Asp159Glu
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*265C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*104C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.91C>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp159Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS

16-70398538-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398538
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398538
    reference: chr 16
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-382G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*215G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1450G>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*106G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1335G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000464207
  ensembl transcript: ENST00000562649
  gene symbol: DDX19A
  hgvsc: ENST00000562649.2:c.*267G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.93G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.232G>T
  hgvsp: ENSP00000460180.1:p.Arg78Ile
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.479G>T
  hgvsp: ENSP00000306117.7:p.Arg160Ile
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.505G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1450G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.386G>T
  hgvsp: ENSP00000410243.2:p.Arg129Ile
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.209G>T
  hgvsp: ENSP00000399208.2:p.Arg70Ile
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg160Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

16-70398560-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398560
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398561
    reference: chr 16
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1424dupG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1424dupG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+16dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1361dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+16dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+16dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+16dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+16dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+16dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+16dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-356dupG
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+16dupG
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

16-70398560-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398560
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398560
    reference: chr 16
allele count: 3
allele frequency: 2.477373323644051e-5
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1357C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+12C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+12C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+12C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-360C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+12C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+12C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+12C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1428C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+12C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+12C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1428C>T
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

16-70398565-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398565
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398565
    reference: chr 16
allele count: 1
allele frequency: 8.263097008758882e-6
allele num: 121020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-355C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+17C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+17C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+17C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+17C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+17C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1423C>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1423C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1362C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+17C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+17C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+17C>G
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-70398567-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398567
    reference: chr 16
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+19G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1421G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-353G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+19G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+19G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1364G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+19G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+19G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1421G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+19G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+19G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+19G>C
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

16-70398567-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398567
    reference: chr 16
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1421G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-353G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+19G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+19G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1364G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1421G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+19G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+19G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+19G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+19G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+19G>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+19G>T
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

16-70398587-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398587
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398587
    reference: chr 16
allele count: 2
allele frequency: 1.658539821541115e-5
allele num: 120588
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1401C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-333C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1384C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1401C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+39C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+39C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

16-70398595-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398595
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398595
    reference: chr 16
allele count: 2
allele frequency: 1.662759182587586e-5
allele num: 120282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+47G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1393G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+47G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-325G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+47G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+47G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1393G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+47G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+47G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1392G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+47G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+47G>A
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15297
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

16-70398596-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398596
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398596
    reference: chr 16
allele count: 1
allele frequency: 8.330417687142833e-6
allele num: 120042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1392C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1393C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-324C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+48C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1392C>T
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6888
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15086
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

16-70398597-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398597
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398597
    reference: chr 16
allele count: 1
allele frequency: 8.336668000533546e-6
allele num: 119952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.103+49G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1391G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.396+49G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.489+49G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1394G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.219+49G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*116+49G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*225+49G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.515+49G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1391G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.242+49G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-323G>A
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15678
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/16-70398876-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398876
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398876
    reference: chr 16
allele count: 1
allele frequency: 8.3301401129567e-6
allele num: 120046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.516-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.220-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.397-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*226-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.490-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.243-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1112C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.104-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1673C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*117-44C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1112C>A
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

16-70398888-C-CCTAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398888
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398892
    reference: chr 16
allele count: 1
allele frequency: 8.309650828472188e-6
allele num: 120342
alternate allele: CCTAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1099_*319-1096dupCTAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.220-31_220-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*226-31_*226-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.104-31_104-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.243-31_243-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.397-31_397-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1686_1689dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-31_354-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1099_608-1096dupCTAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.516-31_516-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.490-31_490-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*117-31_*117-28dupCTAA
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13232
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-70398897-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398897
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398897
    reference: chr 16
allele count: 3
allele frequency: 2.488263689597399e-5
allele num: 120566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.397-23A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*226-23A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.516-23A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1091A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.220-23A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-23A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1694A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.490-23A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*117-23A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.243-23A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1091A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.104-23A>C
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

16-70398898-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398898
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398898
    reference: chr 16
allele count: 6
allele frequency: 4.975454424837468e-5
allele num: 120592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.397-22T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.243-22T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1090T>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*117-22T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.490-22T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.104-22T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-22T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.516-22T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1695T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.220-22T>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1090T>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*226-22T>A
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15998
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD

16-70398899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398899
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398899
    reference: chr 16
allele count: 3
allele frequency: 2.487314695055218e-5
allele num: 120612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-21C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1089C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.220-21C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.104-21C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.243-21C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1696C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1089C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*117-21C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*226-21C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.516-21C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.490-21C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.397-21C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

16-70398901-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398901
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398901
    reference: chr 16
allele count: 2
allele frequency: 1.65694591728526e-5
allele num: 120704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.397-19T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*117-19T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-19T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.243-19T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.490-19T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1087T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*226-19T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.516-19T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1087T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1698T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.220-19T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.104-19T>G
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

16-70398905-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398905
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398905
    reference: chr 16
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1083T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1083T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.104-15T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.243-15T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.516-15T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.354-15T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.220-15T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*117-15T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1702T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.490-15T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*226-15T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.397-15T>C
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

16-70398925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398925
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398925
    reference: chr 16
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.225G>A
  hgvsp: ENST00000443119.2:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.109G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.359G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.248G>A
  hgvsp: ENST00000575878.1:c.248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.402G>A
  hgvsp: ENST00000417604.2:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.495G>A
  hgvsp: ENST00000302243.7:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*122G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1722G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1063G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1063G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.521G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*231G>A
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10980
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu165Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-70398931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398931
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398931
    reference: chr 16
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.231C>T
  hgvsp: ENST00000443119.2:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.408C>T
  hgvsp: ENST00000417604.2:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1057C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*237C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1057C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.254C>T
  hgvsp: ENST00000575878.1:c.254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.365C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*128C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.501C>T
  hgvsp: ENST00000302243.7:c.501C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1728C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.527C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.115C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16579
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu167Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

16-70398933-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398933
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398933
    reference: chr 16
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.233C>T
  hgvsp: ENSP00000399208.2:p.Ser78Phe
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.256C>T
  hgvsp: ENSP00000460180.1:p.Ser86Phe
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.117C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*130C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.367C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.529C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1730C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.410C>T
  hgvsp: ENSP00000410243.2:p.Ser137Phe
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*239C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1055C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1055C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.503C>T
  hgvsp: ENSP00000306117.7:p.Ser168Phe
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser168Phe
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-70398937-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398937
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398937
    reference: chr 16
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1734A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.414A>C
  hgvsp: ENST00000417604.2:c.414A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.533A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1051A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.121A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.260A>C
  hgvsp: ENST00000575878.1:c.260A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*243A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*134A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1051A>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.237A>C
  hgvsp: ENST00000443119.2:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.507A>C
  hgvsp: ENST00000302243.7:c.507A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.371A>C
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro169Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-70398937-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398937
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398937
    reference: chr 16
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.533A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.121A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1051A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.237A>G
  hgvsp: ENST00000443119.2:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*243A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.414A>G
  hgvsp: ENST00000417604.2:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*134A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1051A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.260A>G
  hgvsp: ENST00000575878.1:c.260A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.371A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.507A>G
  hgvsp: ENST00000302243.7:c.507A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1734A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro169Pro
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: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

16-70398938-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398938
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398938
    reference: chr 16
allele count: 3
allele frequency: 2.471984179301253e-5
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1735A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.261A>G
  hgvsp: ENSP00000460180.1:p.Thr88Ala
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1050A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.372A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.122A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.415A>G
  hgvsp: ENSP00000410243.2:p.Thr139Ala
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.508A>G
  hgvsp: ENSP00000306117.7:p.Thr170Ala
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*244A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*135A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.238A>G
  hgvsp: ENSP00000399208.2:p.Thr80Ala
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.534A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1050A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr170Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

16-70398940-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398940
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398940
    reference: chr 16
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.374A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*137A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.263A>G
  hgvsp: ENST00000575878.1:c.263A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*246A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.536A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1048A>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.510A>G
  hgvsp: ENST00000302243.7:c.510A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.417A>G
  hgvsp: ENST00000417604.2:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1737A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1048A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.240A>G
  hgvsp: ENST00000443119.2:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.124A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr170Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-70398951-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398951
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398951
    reference: chr 16
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*148C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1037C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.251C>T
  hgvsp: ENSP00000399208.2:p.Ala84Val
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.274C>T
  hgvsp: ENSP00000460180.1:p.Ala92Val
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*257C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.428C>T
  hgvsp: ENSP00000410243.2:p.Ala143Val
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1037C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.385C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.135C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.521C>T
  hgvsp: ENSP00000306117.7:p.Ala174Val
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1748C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.547C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala174Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

16-70398954-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398954
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398954
    reference: chr 16
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.524T>C
  hgvsp: ENSP00000306117.7:p.Leu175Pro
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*151T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.431T>C
  hgvsp: ENSP00000410243.2:p.Leu144Pro
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1034T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*260T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.277T>C
  hgvsp: ENSP00000460180.1:p.Leu93Pro
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.550T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.254T>C
  hgvsp: ENSP00000399208.2:p.Leu85Pro
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1034T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.388T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1751T>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.138T>C
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu175Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/16-70398961-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398961
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398961
    reference: chr 16
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*267A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.531A>C
  hgvsp: ENST00000302243.7:c.531A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1027A>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.261A>C
  hgvsp: ENST00000443119.2:c.261A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1758A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.438A>C
  hgvsp: ENST00000417604.2:c.438A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1027A>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.284A>C
  hgvsp: ENST00000575878.1:c.284A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.395A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*158A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.557A>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.145A>C
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr177Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-70398970-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398970
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398970
    reference: chr 16
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1767G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*276G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.154G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.540G>C
  hgvsp: ENST00000302243.7:c.540G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1018G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.566G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.404G>C
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.293G>C
  hgvsp: ENST00000575878.1:c.293G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.447G>C
  hgvsp: ENST00000417604.2:c.447G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.270G>C
  hgvsp: ENST00000443119.2:c.270G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1018G>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*167G>C
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val180Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

16-70398987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70398987
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70398987
    reference: chr 16
allele count: 129
allele frequency: 1.062655485444091e-3
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*293A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-1001A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.287A>G
  hgvsp: ENSP00000399208.2:p.Lys96Arg
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.557A>G
  hgvsp: ENSP00000306117.7:p.Lys186Arg
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.310A>G
  hgvsp: ENSP00000460180.1:p.Lys104Arg
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.464A>G
  hgvsp: ENSP00000410243.2:p.Lys155Arg
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.421A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.583A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-1001A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1784A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.171A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*184A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16626
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Lys186Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-70399000-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399000
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399000
    reference: chr 16
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.570A>G
  hgvsp: ENST00000302243.7:c.570A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.596A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.323A>G
  hgvsp: ENST00000575878.1:c.323A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.300A>G
  hgvsp: ENST00000443119.2:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.477A>G
  hgvsp: ENST00000417604.2:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1797A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*197A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.184A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-988A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.434A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-988A>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*306A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu190Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

16-70399002-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399002
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399002
    reference: chr 16
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.572T>G
  hgvsp: ENSP00000306117.7:p.Leu191Arg
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.302T>G
  hgvsp: ENSP00000399208.2:p.Leu101Arg
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*199T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.325T>G
  hgvsp: ENSP00000460180.1:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.436T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.479T>G
  hgvsp: ENSP00000410243.2:p.Leu160Arg
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-986T>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*308T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1799T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.186T>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-986T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.598T>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu191Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

16-70399012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399012
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399012
    reference: chr 16
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.196C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.446C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*209C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.582C>T
  hgvsp: ENST00000302243.7:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.608C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.312C>T
  hgvsp: ENST00000443119.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.335C>T
  hgvsp: ENST00000575878.1:c.335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-976C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.489C>T
  hgvsp: ENST00000417604.2:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1809C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-976C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*318C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala194Ala
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-70399018-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399018
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399018
    reference: chr 16
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*215C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-970C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.202C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.452C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.588C>G
  hgvsp: ENST00000302243.7:c.588C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1815C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*324C>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.495C>G
  hgvsp: ENST00000417604.2:c.495C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-970C>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.341C>G
  hgvsp: ENST00000575878.1:c.341C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.318C>G
  hgvsp: ENST00000443119.2:c.318C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.614C>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala196Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

16-70399018-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399018
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399018
    reference: chr 16
allele count: 14
allele frequency: 1.153877853787192e-4
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*324C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1815C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.318C>T
  hgvsp: ENST00000443119.2:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*215C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.202C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.452C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.341C>T
  hgvsp: ENST00000575878.1:c.341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.495C>T
  hgvsp: ENST00000417604.2:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-970C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.588C>T
  hgvsp: ENST00000302243.7:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-970C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.614C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10936
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13396
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala196Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

16-70399019-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399019
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399019
    reference: chr 16
allele count: 23
allele frequency: 1.895718972025782e-4
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.342G>A
  hgvsp: ENSP00000460180.1:p.Val115Ile
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.496G>A
  hgvsp: ENSP00000410243.2:p.Val166Ile
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.589G>A
  hgvsp: ENSP00000306117.7:p.Val197Ile
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1816G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.319G>A
  hgvsp: ENSP00000399208.2:p.Val107Ile
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*216G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-969G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*325G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.453G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-969G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.203G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.615G>A
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val197Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

16-70399022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399022
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399022
    reference: chr 16
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-966C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*219C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.456C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*328C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.345C>T
  hgvsp: ENSP00000460180.1:p.Arg116Ter
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1819C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.322C>T
  hgvsp: ENSP00000399208.2:p.Arg108Ter
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.206C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.618C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.592C>T
  hgvsp: ENSP00000306117.7:p.Arg198Ter
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.499C>T
  hgvsp: ENSP00000410243.2:p.Arg167Ter
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-966C>T
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg198Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-70399029-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399029
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399029
    reference: chr 16
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.599A>G
  hgvsp: ENSP00000306117.7:p.Asn200Ser
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-959A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.506A>G
  hgvsp: ENSP00000410243.2:p.Asn169Ser
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.329A>G
  hgvsp: ENSP00000399208.2:p.Asn110Ser
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*226A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.625A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.352A>G
  hgvsp: ENSP00000460180.1:p.Asn118Ser
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.463A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*335A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1826A>G
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-959A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.213A>G
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn200Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-70399042-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399042
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399042
    reference: chr 16
allele count: 4
allele frequency: 3.302564441288661e-5
allele num: 121118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.511+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.468+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*231+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.357+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*340+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-946C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-946C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.218+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.604+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.334+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.630+8C>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1839C>A
  variant of: http://identifiers.org/hgnc/25628
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.604+8C>A
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

16-70399042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399042
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399042
    reference: chr 16
allele count: 2
allele frequency: 1.65128222064433e-5
allele num: 121118
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.604+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1839C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*340+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.334+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.468+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.511+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.218+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.357+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-946C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.630+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*231+8C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-946C>T
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13374
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.604+8C>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

16-70399043-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399043
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399043
    reference: chr 16
allele count: 5
allele frequency: 4.128137384412153e-5
allele num: 121120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.468+9G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*231+9G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.357+9G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1840G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.218+9G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.334+9G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-945G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.511+9G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-945G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.604+9G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.630+9G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*340+9G>A
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

16-70399044-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399044
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399044
    reference: chr 16
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-944G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.334+10G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.511+10G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.604+10G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*231+10G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1841G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.357+10G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-944G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.468+10G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.218+10G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.630+10G>A
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*340+10G>A
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS

16-70399049-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70399049
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 70399049
    reference: chr 16
allele count: 6
allele frequency: 4.958431813298514e-5
allele num: 121006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000562140
  gene symbol: DDX19A
  hgvsc: ENST00000562140.2:n.218+15C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000456765
  ensembl transcript: ENST00000569319
  gene symbol: DDX19A
  hgvsc: ENST00000569319.1:c.*231+15C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000568779
  gene symbol: DDX19A
  hgvsc: ENST00000568779.1:n.630+15C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000566574
  gene symbol: DDX19A
  hgvsc: ENST00000566574.1:n.1846C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000410243
  ensembl transcript: ENST00000417604
  gene symbol: DDX19A
  hgvsc: ENST00000417604.2:c.511+15C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000460180
  ensembl transcript: ENST00000575878
  gene symbol: DDX19A
  hgvsc: ENST00000575878.1:c.357+15C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000399208
  ensembl transcript: ENST00000443119
  gene symbol: DDX19A
  hgvsc: ENST00000443119.2:c.334+15C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000455483
  ensembl transcript: ENST00000565116
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000565116.1:c.*319-939C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000306117
  ensembl transcript: ENST00000302243
  gene symbol: DDX19A
  hgvsc: ENST00000302243.7:c.604+15C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl transcript: ENST00000567012
  gene symbol: DDX19A
  hgvsc: ENST00000567012.1:n.468+15C>T
  variant of: http://identifiers.org/hgnc/25628
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000260537
  ensembl protein: ENSP00000454699
  ensembl transcript: ENST00000567706
  gene symbol: RP11-529K1.3
  hgvsc: ENST00000567706.1:c.608-939C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168872
  ensembl protein: ENSP00000457103
  ensembl transcript: ENST00000569771
  gene symbol: DDX19A
  hgvsc: ENST00000569771.1:c.*340+15C>T
  variant of: http://identifiers.org/hgnc/25628
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6467
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3092
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10049
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2817
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29653
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.38e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.925408e6

QD
type: SiteQuality
SIO_000300: 2.756e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.654e0

VQSLOD
type: SiteQuality
SIO_000300: -2.946e0

GenotypeQuality
all individuals: 4071
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 10021
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6465
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.419e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.099e0

DP
type: SiteQuality
SIO_000300: 1.920049e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.26e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9964
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6460
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4063
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.716875871687587e-5
allele num: 11472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.742e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.683e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

DP
type: SiteQuality
SIO_000300: 1.912703e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.182e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.106e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.64e-1

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3958
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6443
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 28202
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.15807759119861e-3
allele num: 10362
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66220
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.746419839329375e-4
allele num: 11452
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

MQRankSum
type: SiteQuality
SIO_000300: -5.98e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.112e0

FS
type: SiteQuality
SIO_000300: 1.687e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

DP
type: SiteQuality
SIO_000300: 1.892737e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

QD
type: SiteQuality
SIO_000300: 1.395e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

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

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6410
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 395
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2841
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8973
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2697
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25979
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66088
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.032e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.159999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.484e0

DP
type: SiteQuality
SIO_000300: 1.843857e6

QD
type: SiteQuality
SIO_000300: 7.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.109e0

GenotypeQuality
all individuals: 2771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25049
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6393
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3743
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.665571235260003e-5
allele num: 10346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.828251e6

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.168e0

QD
type: SiteQuality
SIO_000300: 1.074e1

GenotypeQuality
all individuals: 1841
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3599
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1805
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6382
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3476
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3929
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17252
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65704
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.593e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.963e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.792999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.888e1

DP
type: SiteQuality
SIO_000300: 1.734236e6

GenotypeQuality
all individuals: 4502
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3731
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2685
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13057
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4695
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2450
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2714
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6386
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1627
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3459
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6344
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527370478983382e-5
allele num: 65472
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.828153564899452e-4
allele num: 16410
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.910360884749709e-4
allele num: 10308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.802816901408451e-5
allele num: 11360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.698308e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.461e1

GenotypeQuality
all individuals: 2556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2309
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10502
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6380
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 186
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4813
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5598
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5458
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534872298624754e-5
allele num: 65152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.100536847242558e-5
allele num: 16392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.685301e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e0

VQSLOD
type: SiteQuality
SIO_000300: -1.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.553e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 12709
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9189
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3307
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5732
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 21098
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1872
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.520931914765364e-5
allele num: 66358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

FS
type: SiteQuality
SIO_000300: 6.4e0

DP
type: SiteQuality
SIO_000300: 1.706481e6

MQ
type: SiteQuality
SIO_000300: 6.06e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

QD
type: SiteQuality
SIO_000300: 1.284e1

GenotypeDepth
all individuals: 727
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3516
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24354
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4598
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5717
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 873
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9302
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3253
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506432466632521e-5
allele num: 66382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

FS
type: SiteQuality
SIO_000300: 3.324e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.619e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

DP
type: SiteQuality
SIO_000300: 1.722345e6

VQSLOD
type: SiteQuality
SIO_000300: -7.677e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.622e1

GenotypeDepth
all individuals: 18272
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4591
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5713
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1446
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1885
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26366
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3246
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506160195198361e-5
allele num: 66394
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

DP
type: SiteQuality
SIO_000300: 1.736784e6

MQRankSum
type: SiteQuality
SIO_000300: -6.45e-1

QD
type: SiteQuality
SIO_000300: 1.462e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 6.18e-1

FS
type: SiteQuality
SIO_000300: 1.523e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.096e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.46e-1

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 890
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3538
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5715
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1883
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26783
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 4.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.012138919846983e-5
allele num: 66398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 1.739674e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

VQSLOD
type: SiteQuality
SIO_000300: -1.269e0

QD
type: SiteQuality
SIO_000300: 7.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e-1

GenotypeDepth
all individuals: 67
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27745
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5726
bin: 9.75e1
variant carriers: 10

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

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3569
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4614
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 9
allele frequency: 7.813856572321583e-4
allele num: 11518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505117399157134e-5
allele num: 66440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 8.27e-1

FS
type: SiteQuality
SIO_000300: 1.057e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

QD
type: SiteQuality
SIO_000300: 1.609e1

DP
type: SiteQuality
SIO_000300: 1.750892e6

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

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3606
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1892
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5718
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4644
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9753
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

DP
type: SiteQuality
SIO_000300: 1.771209e6

FS
type: SiteQuality
SIO_000300: 1.417e0

MQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

MQ
type: SiteQuality
SIO_000300: 5.665e1

QD
type: SiteQuality
SIO_000300: 1.646e1

GenotypeDepth
all individuals: 5255
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9764
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29692
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5718
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3612
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4650
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.861e0

FS
type: SiteQuality
SIO_000300: 1.667e0

DP
type: SiteQuality
SIO_000300: 1.773178e6

VQSLOD
type: SiteQuality
SIO_000300: 4.76e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

GenotypeDepth
all individuals: 5256
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1251
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2577
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30082
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9817
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3634
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5721
bin: 9.75e1
variant carriers: 4

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

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

GenotypeQuality
all individuals: 1451
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3276
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4659
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.423654871546292e-4
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.18e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.55e-1

DP
type: SiteQuality
SIO_000300: 1.777819e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.28e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4663
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30170
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 5718
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1896
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9840
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

QD
type: SiteQuality
SIO_000300: 1.073e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.58e-1

DP
type: SiteQuality
SIO_000300: 1.779467e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.475e0

GenotypeDepth
all individuals: 134
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3631
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3279
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5716
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4665
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30165
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.787e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.023e1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.45e-1

DP
type: SiteQuality
SIO_000300: 1.779384e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.686e0

GenotypeDepth
all individuals: 18056
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11884
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9844
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4664
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30166
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5715
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3279
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.779437e6

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.14e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.655e0

GenotypeDepth
all individuals: 725
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2575
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11885
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1896
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30137
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5715
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3280
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4660
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9834
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.779328e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.235e1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 6.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.39e-1

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

GenotypeDepth
all individuals: 19877
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9825
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3629
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3274
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30051
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5711
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1897
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4653
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 1.778289e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

FS
type: SiteQuality
SIO_000300: 5.551e0

VQSLOD
type: SiteQuality
SIO_000300: -5.01e-2

GenotypeDepth
all individuals: 19879
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1450
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5711
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3630
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4652
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30029
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1897
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.122e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.214e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.427e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.778013e6

MQRankSum
type: SiteQuality
SIO_000300: 9.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.56e-1

GenotypeDepth
all individuals: 179
bin: 6.75e1
variant carriers: 49

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 35

GenotypeDepth
all individuals: 17825
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 75
bin: 8.25e1
variant carriers: 39

GenotypeDepth
all individuals: 43
bin: 9.25e1
variant carriers: 27

GenotypeQuality
all individuals: 9786
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6040
bin: 9.75e1
variant carriers: 504

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29908
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 8.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 133
allele frequency: 2.010885999395222e-2
allele num: 6614
num of homozygotes: 3

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

European (Non-Finnish)
type: Population
allele count: 368
allele frequency: 5.520055200552006e-3
allele num: 66666
num of homozygotes: 2

African
type: Population
allele count: 5
allele frequency: 4.812319538017325e-4
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

DP
type: SiteQuality
SIO_000300: 1.797662e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

FS
type: SiteQuality
SIO_000300: 2.078e0

QD
type: SiteQuality
SIO_000300: 1.293e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17812
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3256
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29887
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5579
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

MQ
type: SiteQuality
SIO_000300: 5.882e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.271e0

DP
type: SiteQuality
SIO_000300: 1.775939e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.14e-1

FS
type: SiteQuality
SIO_000300: 3.224e0

GenotypeDepth
all individuals: 1238
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 224
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5579
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 149
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3624
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9839
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.387e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.775841e6

QD
type: SiteQuality
SIO_000300: 1.125e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.073e0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4602
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.1049e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.767957e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 8.109999999999999e0

GenotypeDepth
all individuals: 19667
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5574
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4602
bin: 7.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006433768264085e-5
allele num: 66524
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.1049e1

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.83e-1

DP
type: SiteQuality
SIO_000300: 1.767957e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

QD
type: SiteQuality
SIO_000300: 8.109999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

GenotypeDepth
all individuals: 889
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1861
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9583
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5563
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3555
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28602
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4581
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66492
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -5.51e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.704e1

FS
type: SiteQuality
SIO_000300: 5.934e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.85e-1

DP
type: SiteQuality
SIO_000300: 1.761487e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e0

GenotypeDepth
all individuals: 16505
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4572
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5563
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9484
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28049
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 779
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3536
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504755025881786e-5
allele num: 66456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.006e0

FS
type: SiteQuality
SIO_000300: 1.781e0

QD
type: SiteQuality
SIO_000300: 1.09e1

DP
type: SiteQuality
SIO_000300: 1.757195e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.76e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5563
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 353
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 265
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28049
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9484
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4572
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3536
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66456
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

FS
type: SiteQuality
SIO_000300: 1.781e0

QD
type: SiteQuality
SIO_000300: 1.09e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.006e0

DP
type: SiteQuality
SIO_000300: 1.757195e6

GenotypeDepth
all individuals: 133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5557
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4315
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 664
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3242
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8268
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1826
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1240
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.743983257760725e-4
allele num: 11468
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66232
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.05e-1

DP
type: SiteQuality
SIO_000300: 1.701379e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

FS
type: SiteQuality
SIO_000300: 2.078e0

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.185e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

GenotypeDepth
all individuals: 80
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1304
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5546
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4231
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17624
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3085
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.753463089601964e-4
allele num: 11406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66080
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.629e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 3.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

DP
type: SiteQuality
SIO_000300: 1.671387e6

GenotypeDepth
all individuals: 15391
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1720
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3084
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3470
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3067
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5543
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 149
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7479
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516070345664039e-5
allele num: 65960
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

FS
type: SiteQuality
SIO_000300: 2.569e0

DP
type: SiteQuality
SIO_000300: 1.669761e6

VQSLOD
type: SiteQuality
SIO_000300: -2.365e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.743e1

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5540
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1694
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4139
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16087
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3036
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2754
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3740
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.763718023823472e-5
allele num: 10242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

QD
type: SiteQuality
SIO_000300: 6.54e0

FS
type: SiteQuality
SIO_000300: 4.561e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.666721e6

GenotypeDepth
all individuals: 15093
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8137
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21295
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10126
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 505
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3250
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2473
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66254
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

QD
type: SiteQuality
SIO_000300: 1.524e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.939e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 2.011702e6

GenotypeDepth
all individuals: 356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8225
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23916
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10118
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506841058405159e-5
allele num: 66364
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.11e-1

QD
type: SiteQuality
SIO_000300: 1.44e1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.046e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
SIO_000300: 5.358e1

DP
type: SiteQuality
SIO_000300: 2.03071e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.03e-1

GenotypeDepth
all individuals: 4259
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4591
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8299
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3591
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10119
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3270
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66446
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: 3
allele frequency: 1.87453136715821e-4
allele num: 16004
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.04216e6

VQSLOD
type: SiteQuality
SIO_000300: -4.29e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

FS
type: SiteQuality
SIO_000300: 2.812e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.042e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.09e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeDepth
all individuals: 238
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8310
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4593
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10122
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 25047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 6
allele frequency: 3.747189607794155e-4
allele num: 16012
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

DP
type: SiteQuality
SIO_000300: 2.042909e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.394e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.6e0

GenotypeDepth
all individuals: 219
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4590
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10118
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 224
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8308
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25130
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.886280546469117e-4
allele num: 10394
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.925e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-2

FS
type: SiteQuality
SIO_000300: 1.533e0

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.04e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.072e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.56e-1

DP
type: SiteQuality
SIO_000300: 2.044607e6

QD
type: SiteQuality
SIO_000300: 1.836e1

GenotypeDepth
all individuals: 238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8337
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10119
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1636
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3283
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4595
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16080
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007790176557283e-5
allele num: 66494
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.661e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

QD
type: SiteQuality
SIO_000300: 1.059e1

VQSLOD
type: SiteQuality
SIO_000300: -6.438e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.35e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.046012e6

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 158
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8352
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10118
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25550
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2468
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 2.049186e6

VQSLOD
type: SiteQuality
SIO_000300: -1.02e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.58e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.291e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.094e0

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 542
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10118
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3297
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8413
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2465
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

DP
type: SiteQuality
SIO_000300: 2.058662e6

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.739e0

FS
type: SiteQuality
SIO_000300: 1.686e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.267e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.678e0

GenotypeDepth
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2544
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10117
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3589
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26419
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.351e0

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.617e0

DP
type: SiteQuality
SIO_000300: 2.05998e6

GenotypeDepth
all individuals: 219
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8418
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 10116
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26427
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.084e0

QD
type: SiteQuality
SIO_000300: 1.151e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.552e1

VQSLOD
type: SiteQuality
SIO_000300: -2.162e0

DP
type: SiteQuality
SIO_000300: 2.060261e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.741e0

GenotypeDepth
all individuals: 10980
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10119
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8423
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.292e0

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.57e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

DP
type: SiteQuality
SIO_000300: 2.060678e6

QD
type: SiteQuality
SIO_000300: 1.321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

GenotypeDepth
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10980
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10119
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 8.292e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

DP
type: SiteQuality
SIO_000300: 2.060678e6

QD
type: SiteQuality
SIO_000300: 1.321e1

GenotypeDepth
all individuals: 461
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7418
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26491
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4601
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10119
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3584
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.247e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 2.06083e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.026e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: 7.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.188e1

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1595
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3297
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26497
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10117
bin: 9.75e1
variant carriers: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.912e0

DP
type: SiteQuality
SIO_000300: 2.060846e6

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.85e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

GenotypeDepth
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10118
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26534
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8428
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3582
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

DP
type: SiteQuality
SIO_000300: 2.061527e6

VQSLOD
type: SiteQuality
SIO_000300: 7.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

FS
type: SiteQuality
SIO_000300: 1.155e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

GenotypeDepth
all individuals: 238
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1595
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3582
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10117
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8429
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4602
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.466e0

VQSLOD
type: SiteQuality
SIO_000300: -4.947e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.061459e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.013e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.249e1

GenotypeDepth
all individuals: 4259
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8428
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3582
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1635
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10116
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4601
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.273e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.226e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 2.061508e6

FS
type: SiteQuality
SIO_000300: 3.351e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.174e1

GenotypeDepth
all individuals: 2543
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13385
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3582
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4599
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10117
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 26559
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 9.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 8.77e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

MQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 9.73e0

VQSLOD
type: SiteQuality
SIO_000300: -8.457e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.946e0

DP
type: SiteQuality
SIO_000300: 2.061477e6

GenotypeDepth
all individuals: 604
bin: 9.75e1
variant carriers: 65

GenotypeDepth
all individuals: 163
bin: 9.25e1
variant carriers: 15

GenotypeQuality
all individuals: 26540
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1627
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10187
bin: 9.75e1
variant carriers: 129

GenotypeQuality
all individuals: 2453
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3575
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 115
allele frequency: 1.723414458697998e-3
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.318535152876144e-4
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.845414343395501e-4
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.311258278145695e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

FS
type: SiteQuality
SIO_000300: 1.113e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

DP
type: SiteQuality
SIO_000300: 2.069591e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

GenotypeDepth
all individuals: 219
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 540
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3304
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10072
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26583
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3580
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4593
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.455e0

VQSLOD
type: SiteQuality
SIO_000300: 6.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.060573e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.606e0

QD
type: SiteQuality
SIO_000300: 1.488e1

MQ
type: SiteQuality
SIO_000300: 5.988e1

GenotypeDepth
all individuals: 682
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1002
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3580
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26582
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3304
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8436
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4593
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10071
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.616e0

MQRankSum
type: SiteQuality
SIO_000300: 9.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.060452e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.39e-1

FS
type: SiteQuality
SIO_000300: 2.221e0

QD
type: SiteQuality
SIO_000300: 1.207e1

GenotypeDepth
all individuals: 357
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26548
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3579
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10070
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4593
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8431
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.060066e6

MQRankSum
type: SiteQuality
SIO_000300: -7.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.08e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

GenotypeDepth
all individuals: 13396
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4592
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26511
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 2.060298e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.302e1

FS
type: SiteQuality
SIO_000300: 2.127e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

GenotypeDepth
all individuals: 683
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7414
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10079
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8424
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26511
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4592
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.998200359928014e-5
allele num: 66680
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.635922918434129e-4
allele num: 16502
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.127e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 2.060298e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.302e1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

GenotypeDepth
all individuals: 361
bin: 7.25e1
variant carriers: 4

GenotypeDepth
all individuals: 240
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3576
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10078
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4587
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2459
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

East Asian
type: Population
allele count: 21
allele frequency: 2.426623526692859e-3
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.060644e6

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.443e0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

QD
type: SiteQuality
SIO_000300: 1.373e1

GenotypeDepth
all individuals: 459
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 218
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2460
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10057
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8420
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4589
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3576
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3296
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

FS
type: SiteQuality
SIO_000300: 1.697e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: -1.235e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.57e-1

QD
type: SiteQuality
SIO_000300: 5.52e0

DP
type: SiteQuality
SIO_000300: 2.059376e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeDepth
all individuals: 681
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8409
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4581
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10056
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3571
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.058308e6

FS
type: SiteQuality
SIO_000300: 1.396e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.76e0

QD
type: SiteQuality
SIO_000300: 1.328e1

MQRankSum
type: SiteQuality
SIO_000300: 4.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

GenotypeDepth
all individuals: 231
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 540
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8337
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25706
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10059
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2459
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.0960741282614e-5
allele num: 16404
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.504639778972342e-5
allele num: 66598
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

MQRankSum
type: SiteQuality
SIO_000300: -3.41e-1

DP
type: SiteQuality
SIO_000300: 2.052038e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.78e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

GenotypeDepth
all individuals: 1005
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25706
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8337
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10059
bin: 9.75e1
variant carriers: 2

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 2.052038e6

MQRankSum
type: SiteQuality
SIO_000300: -3.41e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

GenotypeDepth
all individuals: 1600
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 423
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10056
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3281
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8347
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003003003003003e-5
allele num: 66600
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.93e-1

DP
type: SiteQuality
SIO_000300: 2.051601e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.449e1

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

FS
type: SiteQuality
SIO_000300: 3.017e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

GenotypeDepth
all individuals: 252
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10050
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 465
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8340
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3283
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4568
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3559
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.458e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.76e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.365e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.611e0

DP
type: SiteQuality
SIO_000300: 2.050447e6

FS
type: SiteQuality
SIO_000300: 1.773e0

GenotypeDepth
all individuals: 238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4547
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10052
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 2453
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25282
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8308
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3272
bin: 7.25e1
variant carriers: 0