16-78420875-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420875
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420875
    reference: chr 16
allele count: 1
allele frequency: 8.294900295298451e-6
allele num: 120556
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271824A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+30A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+30A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+30A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271824A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+30A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+30A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222689A>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3702
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19666
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-78420881-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420881
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420880
    reference: chr 16
allele count: 4
allele frequency: 3.319336796508058e-5
allele num: 120506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222696delC
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+37delC
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271831delC
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+37delC
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+37delC
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+37delC
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271831delC
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+37delC
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1789
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3687
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: TC
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/16-78420882-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420882
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420882
    reference: chr 16
allele count: 2
allele frequency: 1.661129568106312e-5
allele num: 120400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+37C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+37C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+37C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271831C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+37C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222696C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271831C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+37C>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5649
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

16-78420882-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420882
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420882
    reference: chr 16
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+37C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222696C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+37C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271831C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+37C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+37C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+37C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271831C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23585
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2366
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13558
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum

16-78420882-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420882
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420882
    reference: chr 16
allele count: 7859
allele frequency: 6.527408637873754e-2
allele num: 120400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+37C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271831C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271831C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+37C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222696C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+37C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+37C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+37C>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.25e1
  variant carriers: 290
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 9.75e1
  variant carriers: 776
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 6.75e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 3.75e1
  variant carriers: 1005
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.25e1
  variant carriers: 577
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 4.25e1
  variant carriers: 966
genotype depth: GenotypeDepth
  all individuals: 11720
  bin: 2.75e1
  variant carriers: 558
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 4.75e1
  variant carriers: 848
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.25e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 2.25e1
  variant carriers: 296
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 8.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 11314
  bin: 3.25e1
  variant carriers: 836
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 5.75e1
  variant carriers: 458
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2294
  bin: 9.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3152
  bin: 8.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 2.25e1
  variant carriers: 4
num of homozygotes: 325
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

16-78420883-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420883
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420883
    reference: chr 16
allele count: 2
allele frequency: 1.660412446451699e-5
allele num: 120452
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+38T>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271832T>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+38T>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+38T>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+38T>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222697T>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+38T>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271832T>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18367
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-78420885-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420885
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420885
    reference: chr 16
allele count: 1
allele frequency: 8.303303053954863e-6
allele num: 120434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271834G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+40G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222699G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271834G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+40G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+40G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+40G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+40G>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18366
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6393
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

16-78420886-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420886
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420886
    reference: chr 16
allele count: 91
allele frequency: 7.558139534883721e-4
allele num: 120400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+41C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271835C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+41C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+41C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222700C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+41C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271835C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+41C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12074
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 11407
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4300
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1527
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-78420886-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420886
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420886
    reference: chr 16
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222700C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+41C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271835C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+41C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+41C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271835C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+41C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+41C>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2632
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

16-78420888-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420888
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420888
    reference: chr 16
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+43A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+43A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271837A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+43A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+43A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+43A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222702A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271837A>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2636
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

16-78420888-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420888
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420887
    reference: chr 16
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271839delT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+45delT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+45delT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+45delT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+45delT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222704delT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+45delT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271839delT
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3592
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13241
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2636
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1759
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2640
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1699
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6150
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: AT
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

16-78420890-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420890
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420890
    reference: chr 16
allele count: 4
allele frequency: 3.323915572544457e-5
allele num: 120340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222704T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271839T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271839T>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7046
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6940
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10385
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4263
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

16-78420897-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78420897
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78420897
    reference: chr 16
allele count: 3
allele frequency: 2.497336174746936e-5
allele num: 120128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+222711T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*223+52T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.293+52T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+271846T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.605+52T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.605+52T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+271846T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*402+52T>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10572
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18337
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3321
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1932
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3566
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

16-78458720-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458720
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458720
    reference: chr 16
allele count: 8
allele frequency: 6.624819887709302e-5
allele num: 120758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-47G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309669G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-47G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-47G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260534G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-47G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309669G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-47G>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13444
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2942
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3237
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39142
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

16-78458722-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458722
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458722
    reference: chr 16
allele count: 4
allele frequency: 3.312464805061446e-5
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309671T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260536T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-45T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309671T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-45T>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39142
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3239
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

16-78458732-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458732
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458732
    reference: chr 16
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-35T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-35T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-35T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309681T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260546T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309681T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-35T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-35T>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5273
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

16-78458740-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458740
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458740
    reference: chr 16
allele count: 2
allele frequency: 1.656204971927326e-5
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309689C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-27C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-27C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-27C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260554C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309689C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-27C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-27C>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2944
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

16-78458749-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458749
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458749
    reference: chr 16
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-18G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-18G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309698G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-18G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-18G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260563G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-18G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309698G>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3187
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39146
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

16-78458750-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458750
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458750
    reference: chr 16
allele count: 17476
allele frequency: 1.447120002649796e-1
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309699G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-17G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-17G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-17G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-17G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309699G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260564G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-17G>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 5.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 2.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 6792
  bin: 3.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 9.75e1
  variant carriers: 13618
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 6969
  bin: 3.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 8.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 4.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 6.25e1
  variant carriers: 121
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3207
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39436
  bin: 9.75e1
  variant carriers: 14854
num of homozygotes: 2587
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

16-78458750-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458750
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458750
    reference: chr 16
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309699G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-17G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-17G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-17G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-17G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260564G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309699G>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-17G>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3138
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5224
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1657
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-78458751-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458751
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458751
    reference: chr 16
allele count: 3
allele frequency: 2.484184028352821e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-16A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309700A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-16A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-16A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309700A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-16A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260565A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-16A>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5899
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3808
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-78458753-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458753
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458754
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-10dupT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-10dupT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-10dupT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-10dupT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309706dupT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309706dupT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260571dupT
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-10dupT
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3547
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2011
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-78458758-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458758
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458758
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-9A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-9A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309707A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-9A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-9A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309707A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260572A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-9A>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3547
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34841
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-78458758-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458758
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458758
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309707A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.606-9A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.294-9A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*224-9A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.606-9A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309707A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260572A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*403-9A>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-78458774-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458774
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458774
    reference: chr 16
allele count: 213
allele frequency: 1.763683033866026e-3
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309723C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*231C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.301C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.613C>A
  hgvsp: ENSP00000386161.3:p.His205Asn
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*410C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260588C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.613C>A
  hgvsp: ENSP00000457230.1:p.His205Asn
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309723C>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 9.75e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6406
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His205Asn
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

16-78458774-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458774
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458774
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.301C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*231C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*410C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.613C>G
  hgvsp: ENSP00000386161.3:p.His205Asp
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260588C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.613C>G
  hgvsp: ENSP00000457230.1:p.His205Asp
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309723C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309723C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6406
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3543
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3810
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His205Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-78458775-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458775
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458775
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309724A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.614A>G
  hgvsp: ENSP00000457230.1:p.His205Arg
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*232A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309724A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260589A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*411A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.614A>G
  hgvsp: ENSP00000386161.3:p.His205Arg
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.302A>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34752
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His205Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

16-78458775-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458775
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458775
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*411A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309724A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.302A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.614A>T
  hgvsp: ENSP00000457230.1:p.His205Leu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260589A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309724A>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.614A>T
  hgvsp: ENSP00000386161.3:p.His205Leu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*232A>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34752
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3979
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3826
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His205Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-78458777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458777
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458777
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*413G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.304G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260591G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.616G>A
  hgvsp: ENSP00000457230.1:p.Val206Met
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.616G>A
  hgvsp: ENSP00000386161.3:p.Val206Met
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309726G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309726G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*234G>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3828
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3827
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3979
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val206Met
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-78458779-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458779
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458779
    reference: chr 16
allele count: 25
allele frequency: 2.070084790673026e-4
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*415G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309728G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.618G>A
  hgvsp: ENST00000566780.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.618G>A
  hgvsp: ENST00000408984.3:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*236G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309728G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260593G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.306G>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3827
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val206Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-78458779-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458779
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458779
    reference: chr 16
allele count: 3
allele frequency: 2.484101748807631e-5
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.618G>C
  hgvsp: ENST00000408984.3:c.618G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.306G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309728G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260593G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*236G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.618G>C
  hgvsp: ENST00000566780.1:c.618G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309728G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*415G>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34751
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val206Val
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

16-78458785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458785
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458785
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.312G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.624G>A
  hgvsp: ENST00000408984.3:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260599G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.624G>A
  hgvsp: ENST00000566780.1:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*421G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309734G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*242G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309734G>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6435
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val208Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

16-78458790-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458790
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458790
    reference: chr 16
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.317A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260604A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.629A>G
  hgvsp: ENSP00000457230.1:p.Asn210Ser
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.629A>G
  hgvsp: ENSP00000386161.3:p.Asn210Ser
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*247A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309739A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*426A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309739A>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6437
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3557
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn210Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-78458791-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458791
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458791
    reference: chr 16
allele count: 7
allele frequency: 5.79614142585079e-5
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.630C>T
  hgvsp: ENST00000566780.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*427C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.318C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309740C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.630C>T
  hgvsp: ENST00000408984.3:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260605C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*248C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309740C>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn210Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

16-78458792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458792
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458792
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*428G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.631G>A
  hgvsp: ENSP00000457230.1:p.Ala211Thr
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.631G>A
  hgvsp: ENSP00000386161.3:p.Ala211Thr
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260606G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*249G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309741G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.319G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309741G>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34735
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3830
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala211Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

16-78458796-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458796
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458796
    reference: chr 16
allele count: 13
allele frequency: 1.076426264800861e-4
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309745C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*432C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.323C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260610C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*253C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.635C>T
  hgvsp: ENSP00000457230.1:p.Ala212Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309745C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.635C>T
  hgvsp: ENSP00000386161.3:p.Ala212Val
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala212Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/16-78458799-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458799
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458799
    reference: chr 16
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.638C>A
  hgvsp: ENSP00000386161.3:p.Thr213Asn
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*435C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309748C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260613C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.326C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.638C>A
  hgvsp: ENSP00000457230.1:p.Thr213Asn
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309748C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*256C>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr213Asn
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

16-78458799-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458799
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458799
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.638C>G
  hgvsp: ENSP00000457230.1:p.Thr213Ser
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*256C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*435C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.326C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.638C>G
  hgvsp: ENSP00000386161.3:p.Thr213Ser
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309748C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260613C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309748C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6442
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3980
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34725
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr213Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

16-78458805-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458805
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458805
    reference: chr 16
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309754C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*262C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.332C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260619C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*441C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.644C>G
  hgvsp: ENSP00000457230.1:p.Ala215Gly
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309754C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.644C>G
  hgvsp: ENSP00000386161.3:p.Ala215Gly
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6441
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala215Gly
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum

16-78458805-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458805
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458805
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.644C>T
  hgvsp: ENSP00000457230.1:p.Ala215Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309754C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.644C>T
  hgvsp: ENSP00000386161.3:p.Ala215Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.332C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260619C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*262C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*441C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309754C>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3560
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala215Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

16-78458807-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458807
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458807
    reference: chr 16
allele count: 2305
allele frequency: 1.908586569512296e-2
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309756C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.334C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*443C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.646C>G
  hgvsp: ENSP00000386161.3:p.Leu216Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260621C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309756C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.646C>G
  hgvsp: ENSP00000457230.1:p.Leu216Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*264C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8027
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8313
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8394
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 9.75e1
  variant carriers: 2121
genotype quality: GenotypeQuality
  all individuals: 3558
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3978
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6437
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3828
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu216Val
num of homozygotes: 60
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-78458811-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458811
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458811
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.650C>T
  hgvsp: ENSP00000457230.1:p.Pro217Leu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309760C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309760C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.338C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*447C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.650C>T
  hgvsp: ENSP00000386161.3:p.Pro217Leu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260625C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*268C>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33730
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3689
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro217Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

16-78458812-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458812
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458812
    reference: chr 16
allele count: 3
allele frequency: 2.48406061107891e-5
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260626C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309761C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*269C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.651C>G
  hgvsp: ENST00000566780.1:c.651C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*448C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.651C>G
  hgvsp: ENST00000408984.3:c.651C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.339C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309761C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro217Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

16-78458819-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458819
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458819
    reference: chr 16
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309768C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*276C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.658C>G
  hgvsp: ENSP00000457230.1:p.Leu220Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260633C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.658C>G
  hgvsp: ENSP00000386161.3:p.Leu220Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*455C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309768C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.346C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu220Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

16-78458820-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458820
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458820
    reference: chr 16
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.659T>C
  hgvsp: ENSP00000386161.3:p.Leu220Pro
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.347T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*277T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309769T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*456T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.659T>C
  hgvsp: ENSP00000457230.1:p.Leu220Pro
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309769T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260634T>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu220Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-78458824-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458824
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458824
    reference: chr 16
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.663C>G
  hgvsp: ENST00000408984.3:c.663C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309773C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*460C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.663C>G
  hgvsp: ENST00000566780.1:c.663C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309773C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*281C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.351C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260638C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33729
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3950
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr221Thr
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

16-78458828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458828
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458828
    reference: chr 16
allele count: 4
allele frequency: 3.312135665076842e-5
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*464G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.667G>A
  hgvsp: ENSP00000457230.1:p.Asp223Asn
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.355G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309777G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.667G>A
  hgvsp: ENSP00000386161.3:p.Asp223Asn
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260642G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309777G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*285G>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2083
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp223Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

16-78458830-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458830
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458830
    reference: chr 16
allele count: 118
allele frequency: 9.770800211976681e-4
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*466T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.669T>C
  hgvsp: ENST00000566780.1:c.669T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309779T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.669T>C
  hgvsp: ENST00000408984.3:c.669T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.357T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*287T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260644T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309779T>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 9.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33724
  bin: 9.75e1
  variant carriers: 116
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3949
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2083
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp223Asp
num of homozygotes: 2
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-78458834-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458834
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458834
    reference: chr 16
allele count: 4
allele frequency: 3.312135665076842e-5
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*470C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260648C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309783C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.673C>G
  hgvsp: ENSP00000386161.3:p.Leu225Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309783C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.673C>G
  hgvsp: ENSP00000457230.1:p.Leu225Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.361C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*291C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3983
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu225Val
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS

16-78458837-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458837
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458837
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*473G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.676G>C
  hgvsp: ENSP00000386161.3:p.Glu226Gln
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309786G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.676G>C
  hgvsp: ENSP00000457230.1:p.Glu226Gln
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.364G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*294G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260651G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309786G>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4156
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu226Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-78458839-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458839
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458839
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.366G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260653G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309788G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*296G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309788G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.678G>A
  hgvsp: ENST00000408984.3:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*475G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.678G>A
  hgvsp: ENST00000566780.1:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33680
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu226Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

16-78458844-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458844
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458844
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309793C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.683C>T
  hgvsp: ENSP00000457230.1:p.Thr228Ile
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*301C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260658C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.683C>T
  hgvsp: ENSP00000386161.3:p.Thr228Ile
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.371C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*480C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309793C>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33679
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3956
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr228Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/16-78458850-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458850
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458850
    reference: chr 16
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309799A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.377A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*486A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.689A>C
  hgvsp: ENSP00000386161.3:p.Gln230Pro
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309799A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*307A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.689A>C
  hgvsp: ENSP00000457230.1:p.Gln230Pro
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260664A>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4155
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln230Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-78458851-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458851
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458851
    reference: chr 16
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309800A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.690A>C
  hgvsp: ENSP00000386161.3:p.Gln230His
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.690A>C
  hgvsp: ENSP00000457230.1:p.Gln230His
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.378A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*308A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260665A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*487A>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309800A>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6724
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln230His
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-78458851-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458851
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458851
    reference: chr 16
allele count: 9
allele frequency: 7.452428663696736e-5
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.690A>G
  hgvsp: ENST00000408984.3:c.690A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*487A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.690A>G
  hgvsp: ENST00000566780.1:c.690A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309800A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309800A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.378A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*308A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260665A>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6724
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4155
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln230Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

16-78458852-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458852
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458852
    reference: chr 16
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454331
  ensembl transcript: ENST00000566662
  gene symbol: WWOX
  hgvsc: ENST00000566662.1:c.*309G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.691G>C
  hgvsp: ENSP00000457230.1:p.Val231Leu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*488G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.691G>C
  hgvsp: ENSP00000386161.3:p.Val231Leu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260666G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309801G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.379G>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309801G>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3698
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val231Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-78458857-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458857
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458857
    reference: chr 16
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309806T>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.384T>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.696T>A
  hgvsp: ENSP00000457230.1:p.Asn232Lys
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260671T>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.696T>A
  hgvsp: ENSP00000386161.3:p.Asn232Lys
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*493T>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309806T>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn232Lys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-78458858-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458858
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458858
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.697C>A
  hgvsp: ENSP00000457230.1:p.His233Asn
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.697C>A
  hgvsp: ENSP00000386161.3:p.His233Asn
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.385C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309807C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260672C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309807C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*494C>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33670
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His233Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

16-78458860-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458860
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458860
    reference: chr 16
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309809T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*496T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.699T>C
  hgvsp: ENST00000408984.3:c.699T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.387T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260674T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.699T>C
  hgvsp: ENST00000566780.1:c.699T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309809T>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3985
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His233His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-78458861-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458861
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458861
    reference: chr 16
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*497C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309810C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.700C>A
  hgvsp: ENSP00000386161.3:p.Leu234Met
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.700C>A
  hgvsp: ENSP00000457230.1:p.Leu234Met
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309810C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.388C>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260675C>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3985
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33670
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu234Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-78458866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458866
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458866
    reference: chr 16
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.705G>A
  hgvsp: ENST00000408984.3:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.393G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309815G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*502G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260680G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.705G>A
  hgvsp: ENST00000566780.1:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309815G>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3701
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly235Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

16-78458867-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458867
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458867
    reference: chr 16
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.394C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309816C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260681C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309816C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.706C>T
  hgvsp: ENSP00000386161.3:p.His236Tyr
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.706C>T
  hgvsp: ENSP00000457230.1:p.His236Tyr
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*503C>T
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3956
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3699
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His236Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-78458869-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458869
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458869
    reference: chr 16
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309818C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*505C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.708C>G
  hgvsp: ENSP00000386161.3:p.His236Gln
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.708C>G
  hgvsp: ENSP00000457230.1:p.His236Gln
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260683C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.396C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309818C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6724
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33668
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His236Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

16-78458872-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458872
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458872
    reference: chr 16
allele count: 11
allele frequency: 9.108674770627008e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.711C>G
  hgvsp: ENSP00000386161.3:p.Phe237Leu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*508C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.399C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309821C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260686C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.711C>G
  hgvsp: ENSP00000457230.1:p.Phe237Leu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309821C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33668
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3699
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3985
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe237Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-78458874-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458874
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458874
    reference: chr 16
allele count: 15
allele frequency: 1.24209201417641e-4
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309823A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260688A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.713A>G
  hgvsp: ENSP00000386161.3:p.Tyr238Cys
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*510A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.401A>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.713A>G
  hgvsp: ENSP00000457230.1:p.Tyr238Cys
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309823A>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33666
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr238Cys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-78458876-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458876
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458876
    reference: chr 16
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.403C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309825C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260690C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.715C>G
  hgvsp: ENSP00000386161.3:p.Leu239Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.715C>G
  hgvsp: ENSP00000457230.1:p.Leu239Val
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309825C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*512C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33661
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu239Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

16-78458876-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458876
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458876
    reference: chr 16
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309825C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.715C>T
  hgvsp: ENSP00000457230.1:p.Leu239Phe
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.403C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*512C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260690C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309825C>T
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.715C>T
  hgvsp: ENSP00000386161.3:p.Leu239Phe
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33661
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu239Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

16-78458878-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458878
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458878
    reference: chr 16
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.405T>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260692T>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*514T>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309827T>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.717T>A
  hgvsp: ENST00000408984.3:c.717T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.717T>A
  hgvsp: ENST00000566780.1:c.717T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309827T>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3957
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33660
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu239Leu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-78458878-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458878
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458878
    reference: chr 16
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.405T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260692T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*514T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309827T>C
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.717T>C
  hgvsp: ENST00000566780.1:c.717T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.717T>C
  hgvsp: ENST00000408984.3:c.717T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309827T>C
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6723
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu239Leu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

16-78458882-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458882
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458882
    reference: chr 16
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.721C>G
  hgvsp: ENSP00000457230.1:p.Gln241Glu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260696C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*518C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.721C>G
  hgvsp: ENSP00000386161.3:p.Gln241Glu
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309831C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309831C>G
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.409C>G
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln241Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

16-78458884-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 78458884
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 78458884
    reference: chr 16
allele count: 5
allele frequency: 4.140306713921367e-5
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000445210
  ensembl transcript: ENST00000539474
  gene symbol: WWOX
  hgvsc: ENST00000539474.2:c.409+309833G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384238
  ensembl transcript: ENST00000402655
  gene symbol: WWOX
  hgvsc: ENST00000402655.2:c.409+309833G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000386161
  ensembl transcript: ENST00000408984
  gene symbol: WWOX
  hgvsc: ENST00000408984.3:c.723G>A
  hgvsp: ENST00000408984.3:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000457230
  ensembl transcript: ENST00000566780
  gene symbol: WWOX
  hgvsc: ENST00000566780.1:c.723G>A
  hgvsp: ENST00000566780.1:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000384495
  ensembl transcript: ENST00000406884
  gene symbol: WWOX
  hgvsc: ENST00000406884.2:c.516+260698G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186153
  ensembl transcript: ENST00000562639
  gene symbol: WWOX
  hgvsc: ENST00000562639.1:n.411G>A
  variant of: http://identifiers.org/hgnc/12799
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186153
  ensembl protein: ENSP00000454788
  ensembl transcript: ENST00000569332
  gene symbol: WWOX
  hgvsc: ENST00000569332.1:c.*520G>A
  variant of: http://identifiers.org/hgnc/12799
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3959
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln241Gln
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6824
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16230
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2773
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
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: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.102e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 2.50188e6

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

GenotypeQuality
all individuals: 2771
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 177
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14763
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6295
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19666
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2694
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4403
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502341217433065e-5
allele num: 66632
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: 11538
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.72e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 2.480075e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

QD
type: SiteQuality
SIO_000300: 1.282e1

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23585
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 900
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13558
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
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: 2
allele frequency: 3.004897983713453e-5
allele num: 66558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

QD
type: SiteQuality
SIO_000300: 1.544e1

VQSLOD
type: SiteQuality
SIO_000300: 6.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.398e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

DP
type: SiteQuality
SIO_000300: 2.530573e6

GenotypeQuality
all individuals: 3792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5649
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

DP
type: SiteQuality
SIO_000300: 2.530573e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.4e0

QD
type: SiteQuality
SIO_000300: 1.544e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.398e0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 23585
bin: 9.75e1
variant carriers: 7452

GenotypeQuality
all individuals: 13558
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 525
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 313
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 900
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 948
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 451
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3792
bin: 7.75e1
variant carriers: 7

GenotypeQuality
all individuals: 5649
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1495
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2366
bin: 7.25e1
variant carriers: 7

Latino
type: Population
allele count: 429
allele frequency: 3.721374045801527e-2
allele num: 11528
num of homozygotes: 6

European (Finnish)
type: Population
allele count: 604
allele frequency: 9.148742805210543e-2
allele num: 6602
num of homozygotes: 29

East Asian
type: Population
allele count: 3
allele frequency: 3.504672897196261e-4
allele num: 8560
num of homozygotes: 0

South Asian
type: Population
allele count: 909
allele frequency: 5.523821098687409e-2
allele num: 16456
num of homozygotes: 38

Other
type: Population
allele count: 63
allele frequency: 7.000000000000001e-2
allele num: 900
num of homozygotes: 6

African
type: Population
allele count: 230
allele frequency: 2.347897100857493e-2
allele num: 9796
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 5621
allele frequency: 8.445265783226659e-2
allele num: 66558
num of homozygotes: 241

VQSLOD
type: SiteQuality
SIO_000300: 6.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.398e0

DP
type: SiteQuality
SIO_000300: 2.530573e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 1.544e1

GenotypeQuality
all individuals: 6475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15281
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3616
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.041232904674423e-4
allele num: 9798
num of homozygotes: 1

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: 8560
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.433029e6

VQSLOD
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

QD
type: SiteQuality
SIO_000300: 2.889e1

GenotypeQuality
all individuals: 1429
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2643
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14408
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2677
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4330
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.082725060827251e-5
allele num: 16440
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.195e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.967e-1

QD
type: SiteQuality
SIO_000300: 1.742e1

DP
type: SiteQuality
SIO_000300: 2.423319e6

GenotypeQuality
all individuals: 3589
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 18409
bin: 9.75e1
variant carriers: 91

GenotypeQuality
all individuals: 6311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13985
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2632
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 82
allele frequency: 1.231564086389715e-3
allele num: 66582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.210653753026634e-3
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.418446e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

QD
type: SiteQuality
SIO_000300: 1.502e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.334e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4300
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3589
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13985
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18409
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1696
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: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 2.418446e6

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.334e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

GenotypeQuality
all individuals: 2640
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13241
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1759
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6150
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.65e-1

DP
type: SiteQuality
SIO_000300: 2.409005e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.025e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

QD
type: SiteQuality
SIO_000300: 1.619e1

GenotypeQuality
all individuals: 642
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 689
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1014
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.409005e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.025e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: -1.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.619e1

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11459
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5708
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2635
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2591
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18340
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2301
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.82570593962999e-4
allele num: 16432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 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: 8536
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.313e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-1

FS
type: SiteQuality
SIO_000300: 4.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

DP
type: SiteQuality
SIO_000300: 2.396785e6

QD
type: SiteQuality
SIO_000300: 1.352e1

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.828599292941607e-4
allele num: 16406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.383839e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.022e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.535e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3185
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1681
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5237
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3171
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.276437847866419e-4
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
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: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
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: 900
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.067e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.361e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.377e1

DP
type: SiteQuality
SIO_000300: 5.699612e6

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5239
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1684
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2944
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 4.083299305839118e-4
allele num: 9796
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: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

DP
type: SiteQuality
SIO_000300: 5.698705e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

FS
type: SiteQuality
SIO_000300: 1.286e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.35e0

QD
type: SiteQuality
SIO_000300: 1.43e1

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3242
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2945
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1685
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 16512
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: 66732
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020616452337212e-4
allele num: 9798
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 5.698808e6

VQSLOD
type: SiteQuality
SIO_000300: -1.632e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.630000000000001e0

GenotypeQuality
all individuals: 39143
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3243
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1684
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3187
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 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: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.041232904674423e-4
allele num: 9798
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.115e1

FS
type: SiteQuality
SIO_000300: 6.514e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 5.699065e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.239e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.492e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

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

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5304
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2945
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.75e1
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: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

VQSLOD
type: SiteQuality
SIO_000300: -5.639e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.138e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 7.865e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.144e0

DP
type: SiteQuality
SIO_000300: 5.69908e6

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

GenotypeQuality
all individuals: 1657
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3138
bin: 8.25e1
variant carriers: 4

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

GenotypeQuality
all individuals: 5224
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1651
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3141
bin: 9.25e1
variant carriers: 7

African
type: Population
allele count: 6002
allele frequency: 6.123240155070394e-1
allele num: 9802
num of homozygotes: 1846

European (Finnish)
type: Population
allele count: 656
allele frequency: 9.918355004535834e-2
allele num: 6614
num of homozygotes: 35

Other
type: Population
allele count: 111
allele frequency: 1.233333333333333e-1
allele num: 900
num of homozygotes: 14

East Asian
type: Population
allele count: 1629
allele frequency: 1.889352818371607e-1
allele num: 8622
num of homozygotes: 169

Latino
type: Population
allele count: 1328
allele frequency: 1.147201105736006e-1
allele num: 11576
num of homozygotes: 80

South Asian
type: Population
allele count: 2500
allele frequency: 1.514050387596899e-1
allele num: 16512
num of homozygotes: 222

European (Non-Finnish)
type: Population
allele count: 5250
allele frequency: 7.866582756450598e-2
allele num: 66738
num of homozygotes: 221

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.99e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.558e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.757e-1

FS
type: SiteQuality
SIO_000300: 1.126e0

DP
type: SiteQuality
SIO_000300: 6.555098e6

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2918
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3207
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39436
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.22e0

VQSLOD
type: SiteQuality
SIO_000300: 4.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

DP
type: SiteQuality
SIO_000300: 6.555098e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

FS
type: SiteQuality
SIO_000300: 1.126e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.757e-1

QD
type: SiteQuality
SIO_000300: 1.558e1

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

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

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3809
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6391
bin: 6.25e1
variant carriers: 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: 900
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: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319109461966605e-4
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.49e0

QD
type: SiteQuality
SIO_000300: 1.466e1

DP
type: SiteQuality
SIO_000300: 3.632238e6

FS
type: SiteQuality
SIO_000300: 3.258e0

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.163e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6395
bin: 6.25e1
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: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 4.04e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.111e0

DP
type: SiteQuality
SIO_000300: 3.630769e6

MQRankSum
type: SiteQuality
SIO_000300: -1.112e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 5.54e0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6396
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3809
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3964
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 900
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.539999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 2.423e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 3.630827e6

QD
type: SiteQuality
SIO_000300: 1.691e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

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

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
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: 34841
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 3964
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.539999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.691e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 2.423e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 3.630827e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34844
bin: 9.75e1
variant carriers: 212

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3810
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

Latino
type: Population
allele count: 7
allele frequency: 6.046993780234969e-4
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 203
allele frequency: 2.071005917159763e-2
allele num: 9802
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.54e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.231e0

VQSLOD
type: SiteQuality
SIO_000300: 6.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.634279e6

QD
type: SiteQuality
SIO_000300: 1.315e1

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

GenotypeQuality
all individuals: 34844
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
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variant carriers: 0

GenotypeQuality
all individuals: 3809
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.75e1
variant carriers: 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: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.29e0

QD
type: SiteQuality
SIO_000300: 1.315e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.54e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.231e0

DP
type: SiteQuality
SIO_000300: 3.634279e6

GenotypeQuality
all individuals: 3826
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3979
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6431
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3555
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 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: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.588273e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.331e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
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: 66740
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.22e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.49e-1

DP
type: SiteQuality
SIO_000300: 3.588273e6

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

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1997
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 34751
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2013
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6431
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
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: 900
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.315e0

QD
type: SiteQuality
SIO_000300: 1.378e1

FS
type: SiteQuality
SIO_000300: 1.5757e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: -9.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.466e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.646000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 3.587672e6

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

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

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34751
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 3979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3828
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 25
allele frequency: 2.550499897980004e-3
allele num: 9802
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: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 3.587813e6

QD
type: SiteQuality
SIO_000300: 1.188e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.683e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

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

GenotypeQuality
all individuals: 6433
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3827
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3555
bin: 7.75e1
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GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3828
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.040399918384003e-4
allele num: 9802
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: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.683e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 3.587813e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.188e1

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34738
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3830
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3829
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3556
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3980
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 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: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.088e1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

VQSLOD
type: SiteQuality
SIO_000300: 4.76e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

FS
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.021e0

DP
type: SiteQuality
SIO_000300: 3.581011e6

GenotypeQuality
all individuals: 3830
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3830
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34738
bin: 9.75e1
variant carriers: 2

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

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

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

GenotypeQuality
all individuals: 2015
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 900
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: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.359e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

DP
type: SiteQuality
SIO_000300: 3.580725e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 3557
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34738
bin: 9.75e1
variant carriers: 7

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

GenotypeQuality
all individuals: 3979
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.477857639693948e-4
allele num: 8626
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 5.38e-1

QD
type: SiteQuality
SIO_000300: 1.238e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 3.580368e6

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2015
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3557
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 6439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3831
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 900
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: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.31e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

DP
type: SiteQuality
SIO_000300: 3.578487e6

GenotypeQuality
all individuals: 3979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
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variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 34735
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 6440
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.798022175606832e-4
allele num: 66740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.26e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 1.819e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.289e1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.97e-1

DP
type: SiteQuality
SIO_000300: 3.578419e6

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6442
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34725
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2015
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 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: 900
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.357e0

DP
type: SiteQuality
SIO_000300: 3.575011e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.37e0

QD
type: SiteQuality
SIO_000300: 1.433e1

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

GenotypeQuality
all individuals: 3830
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2015
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variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

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

GenotypeQuality
all individuals: 1998
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variant carriers: 0

GenotypeQuality
all individuals: 3560
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

QD
type: SiteQuality
SIO_000300: 1.433e1

DP
type: SiteQuality
SIO_000300: 3.575011e6

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.357e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 3.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3560
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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: 900
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: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.425e1

DP
type: SiteQuality
SIO_000300: 3.574406e6

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.964e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 4.349e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.744e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.744e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.425e1

FS
type: SiteQuality
SIO_000300: 4.349e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.964e0

DP
type: SiteQuality
SIO_000300: 3.574406e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2245

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2013
bin: 8.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 827
allele frequency: 1.239136949355709e-2
allele num: 66740
num of homozygotes: 7

Latino
type: Population
allele count: 166
allele frequency: 1.434001382170007e-2
allele num: 11576
num of homozygotes: 2

African
type: Population
allele count: 1006
allele frequency: 1.026321158947154e-1
allele num: 9802
num of homozygotes: 43

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.814333232537043e-3
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 18
allele frequency: 2.0e-2
allele num: 900
num of homozygotes: 1

South Asian
type: Population
allele count: 276
allele frequency: 1.671511627906977e-2
allele num: 16512
num of homozygotes: 7

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.445e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.994e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.62e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.89e0

DP
type: SiteQuality
SIO_000300: 3.596097e6

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2094
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
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: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 66740
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.893e0

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

QD
type: SiteQuality
SIO_000300: 1.451e1

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.102764e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

South Asian
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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: 900
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.508e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.94e-1

DP
type: SiteQuality
SIO_000300: 3.1025e6

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-2

QD
type: SiteQuality
SIO_000300: 1.101e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 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: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

FS
type: SiteQuality
SIO_000300: 3.499e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
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SIO_000300: -3.192e0

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

DP
type: SiteQuality
SIO_000300: 3.101791e6

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.604e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Finnish)
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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: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 6.739e0

MQRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.101458e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.509e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.49e0

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

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

South Asian
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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: 900
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 3.602e0

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.10123e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
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Latino
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allele frequency: 3.456022118541559e-4
allele num: 11574
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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DP
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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Other
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allele num: 900
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European (Finnish)
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allele frequency: 1.239794375566979e-2
allele num: 6614
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European (Non-Finnish)
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allele frequency: 5.244231345519928e-4
allele num: 66740
num of homozygotes: 1

MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 4.080799836768007e-4
allele num: 9802
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 0.0e0
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Other
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ClippingRankSum
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SIO_000300: -9.89e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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African
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European (Finnish)
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num of homozygotes: 0

Other
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VQSLOD
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
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num of homozygotes: 0

European (Finnish)
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Latino
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African
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Other
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MQ
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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QD
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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FS
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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Latino
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8626
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

ClippingRankSum
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MQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
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DP
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FS
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 2.52e0

MQ
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SIO_000300: 5.975e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 4.77e0

QD
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 0.0e0
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South Asian
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Other
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allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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DP
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

InbreedingCoeff
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BaseQRankSum
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DP
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VQSLOD
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FS
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MQRankSum
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MQ
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QD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: 1.22e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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South Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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

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

European (Finnish)
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Other
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South Asian
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African
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European (Non-Finnish)
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allele num: 66740
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East Asian
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Latino
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FS
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

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

QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.87e0

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

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

GenotypeQuality
all individuals: 3987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6723
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 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: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

DP
type: SiteQuality
SIO_000300: 3.067e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.292e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 1.936e0

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

QD
type: SiteQuality
SIO_000300: 1.431e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Finnish)
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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: 11574
num of homozygotes: 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: 8626
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.431e1

FS
type: SiteQuality
SIO_000300: 1.936e0

DP
type: SiteQuality
SIO_000300: 3.067e6

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.292e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3700
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.242e1

DP
type: SiteQuality
SIO_000300: 3.066664e6

MQRankSum
type: SiteQuality
SIO_000300: 2.43e0

VQSLOD
type: SiteQuality
SIO_000300: -8.989999999999999e-2

FS
type: SiteQuality
SIO_000300: 4.035e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 4.035e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.989999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.242e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

DP
type: SiteQuality
SIO_000300: 3.066664e6

MQRankSum
type: SiteQuality
SIO_000300: 2.43e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.281e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.066321e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.089e0

FS
type: SiteQuality
SIO_000300: 2.098e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.1e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0