1-160208449-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208449
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208449
    reference: chr 1
allele count: 1
allele frequency: 8.32279113123377e-6
allele num: 120152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.812A>G
  hgvsp: ENSP00000318227.2:p.Gln271Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.812A>G
  hgvsp: ENSP00000476407.1:p.Gln271Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.327A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1274A>G
  hgvsp: ENSP00000476284.1:p.Gln425Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1274A>G
  hgvsp: ENSP00000451235.1:p.Gln425Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.812A>G
  hgvsp: ENSP00000357052.3:p.Gln271Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.812A>G
  hgvsp: ENSP00000357053.1:p.Gln271Arg
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6722
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln271Arg
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: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

1-160208452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208452
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208452
    reference: chr 1
allele count: 1
allele frequency: 8.328613785521537e-6
allele num: 120068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.809C>T
  hgvsp: ENSP00000476407.1:p.Thr270Ile
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.809C>T
  hgvsp: ENSP00000357053.1:p.Thr270Ile
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1271C>T
  hgvsp: ENSP00000451235.1:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.809C>T
  hgvsp: ENSP00000318227.2:p.Thr270Ile
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.324C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.809C>T
  hgvsp: ENSP00000357052.3:p.Thr270Ile
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1271C>T
  hgvsp: ENSP00000476284.1:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr270Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

1-160208466-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208466
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208466
    reference: chr 1
allele count: 5
allele frequency: 4.175504818532561e-5
allele num: 119746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.795A>G
  hgvsp: ENST00000326837.2:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1257A>G
  hgvsp: ENST00000608310.1:c.1257A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.310A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1257A>G
  hgvsp: ENST00000556710.1:c.1257A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.795A>G
  hgvsp: ENST00000368074.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.795A>G
  hgvsp: ENST00000461888.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.795A>G
  hgvsp: ENST00000368073.3:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23952
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23173
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1741
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala265Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

1-160208472-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208472
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208472
    reference: chr 1
allele count: 1073
allele frequency: 8.969621988530921e-3
allele num: 119626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1251A>G
  hgvsp: ENST00000608310.1:c.1251A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.789A>G
  hgvsp: ENST00000461888.1:c.789A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.789A>G
  hgvsp: ENST00000368073.3:c.789A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.789A>G
  hgvsp: ENST00000326837.2:c.789A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.789A>G
  hgvsp: ENST00000368074.1:c.789A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.304A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1251A>G
  hgvsp: ENST00000556710.1:c.1251A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 3.25e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 3.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.25e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22976
  bin: 2.75e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24174
  bin: 2.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 1.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 6161
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 9.75e1
  variant carriers: 1026
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 4.25e1
  variant carriers: 1
hgvs: p.Arg263Arg
num of homozygotes: 27
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/1-160208483-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208483
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208483
    reference: chr 1
allele count: 1
allele frequency: 8.392923087252828e-6
allele num: 119148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.778G>T
  hgvsp: ENSP00000357053.1:p.Gly260Trp
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.293G>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.778G>T
  hgvsp: ENSP00000357052.3:p.Gly260Trp
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.778G>T
  hgvsp: ENSP00000318227.2:p.Gly260Trp
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.778G>T
  hgvsp: ENSP00000476407.1:p.Gly260Trp
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1240G>T
  hgvsp: ENSP00000451235.1:p.Gly414Trp
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1240G>T
  hgvsp: ENSP00000476284.1:p.Gly414Trp
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1540
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly260Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

1-160208484-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208484
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208484
    reference: chr 1
allele count: 5
allele frequency: 4.197800352615229e-5
allele num: 119110
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.777C>T
  hgvsp: ENST00000368073.3:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.777C>T
  hgvsp: ENST00000368074.1:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1239C>T
  hgvsp: ENST00000556710.1:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1239C>T
  hgvsp: ENST00000608310.1:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.777C>T
  hgvsp: ENST00000326837.2:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.777C>T
  hgvsp: ENST00000461888.1:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.292C>T
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22738
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5988
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp259Asp
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

1-160208487-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208487
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208487
    reference: chr 1
allele count: 3
allele frequency: 2.520584775667955e-5
allele num: 119020
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.774T>C
  hgvsp: ENST00000368073.3:c.774T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.289T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.774T>C
  hgvsp: ENST00000368074.1:c.774T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1236T>C
  hgvsp: ENST00000556710.1:c.1236T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.774T>C
  hgvsp: ENST00000461888.1:c.774T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.774T>C
  hgvsp: ENST00000326837.2:c.774T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1236T>C
  hgvsp: ENST00000608310.1:c.1236T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24969
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg258Arg
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: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-160208516-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208516
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208516
    reference: chr 1
allele count: 1
allele frequency: 8.534316486592589e-6
allele num: 117174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.745G>T
  hgvsp: ENSP00000318227.2:p.Gly249Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1207G>T
  hgvsp: ENSP00000451235.1:p.Gly403Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1207G>T
  hgvsp: ENSP00000476284.1:p.Gly403Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.745G>T
  hgvsp: ENSP00000357052.3:p.Gly249Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.745G>T
  hgvsp: ENSP00000476407.1:p.Gly249Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.260G>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.745G>T
  hgvsp: ENSP00000357053.1:p.Gly249Cys
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24948
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1981
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4001
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly249Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum

1-160208519-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208519
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208519
    reference: chr 1
allele count: 1
allele frequency: 8.548762139242238e-6
allele num: 116976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.742A>G
  hgvsp: ENSP00000318227.2:p.Ser248Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.742A>G
  hgvsp: ENSP00000357052.3:p.Ser248Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1204A>G
  hgvsp: ENSP00000451235.1:p.Ser402Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1204A>G
  hgvsp: ENSP00000476284.1:p.Ser402Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.742A>G
  hgvsp: ENSP00000476407.1:p.Ser248Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.257A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.742A>G
  hgvsp: ENSP00000357053.1:p.Ser248Gly
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser248Gly
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-160208541-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208541
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208541
    reference: chr 1
allele count: 1
allele frequency: 8.900439681720277e-6
allele num: 112354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-4C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-4C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-4C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-4C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-4C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-4C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.235C>T
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9680
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19339
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9676
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4141
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1978
  bin: 9.75e1
  variant carriers: 1
hgvs: c.724-4C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

1-160208543-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208543
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208543
    reference: chr 1
allele count: 2
allele frequency: 1.786001321640978e-5
allele num: 111982
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-6C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-6C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-6C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-6C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.233C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-6C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-6C>T
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32075
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2553
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 3.25e1
  variant carriers: 0
hgvs: c.724-6C>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

1-160208544-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208544
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208544
    reference: chr 1
allele count: 3
allele frequency: 2.687497760418533e-5
allele num: 111628
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-7A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.232A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-7A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-7A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-7A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-7A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-7A>G
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16908
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3938
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10867
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 7.25e1
  variant carriers: 0
hgvs: c.724-7A>G
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

1-160208551-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208551
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208551
    reference: chr 1
allele count: 1
allele frequency: 9.054526357726228e-6
allele num: 110442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-14T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-14T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-14T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-14T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-14T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.225T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-14T>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4273
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12633
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

1-160208554-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208554
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208555
    reference: chr 1
allele count: 1
allele frequency: 9.211665653383444e-6
allele num: 108558
alternate allele: GA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-18dupT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-18dupT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-18dupT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.221dupT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-18dupT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-18dupT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-18dupT
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13164
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15051
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4033
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2676
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13395
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

1-160208563-GAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208563
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208561
    reference: chr 1
allele count: 1
allele frequency: 9.23924090396733e-6
allele num: 108234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.211_212delGT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-28_1186-27delGT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-28_724-27delGT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-28_724-27delGT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-28_724-27delGT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-28_724-27delGT
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-28_1186-27delGT
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19449
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3823
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15039
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4943
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: GAC
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-160208567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208567
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208567
    reference: chr 1
allele count: 3
allele frequency: 2.790957298353335e-5
allele num: 107490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.209G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-30G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-30G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-30G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-30G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-30G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-30G>A
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16750
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4660
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15414
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-160208571-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208571
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208571
    reference: chr 1
allele count: 11
allele frequency: 1.02803738317757e-4
allele num: 107000
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-34T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-34T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-34T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.205T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-34T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-34T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-34T>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21081
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11825
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15539
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1268
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

1-160208574-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208574
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208574
    reference: chr 1
allele count: 1
allele frequency: 9.449652252797097e-6
allele num: 105824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-37C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-37C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-37C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-37C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-37C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-37C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.202C>A
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6282
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9148
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5796
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6523
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

1-160208578-TGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208578
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208576
    reference: chr 1
allele count: 2
allele frequency: 1.905342580595991e-5
allele num: 104968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-43_724-42delTC
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-43_724-42delTC
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.196_197delTC
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-43_1186-42delTC
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-43_724-42delTC
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-43_724-42delTC
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-43_1186-42delTC
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6278
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5902
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9442
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8824
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: TGA
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

1-160208579-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160208579
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160208579
    reference: chr 1
allele count: 11
allele frequency: 1.053316990960625e-4
allele num: 104432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.724-42C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000132716
  ensembl transcript: ENST00000466253
  gene symbol: DCAF8
  hgvsc: ENST00000466253.1:n.197C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.724-42C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.724-42C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.724-42C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1186-42C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1186-42C>T
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20566
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16600
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6235
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9489
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14369
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2889
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2692
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7996
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-160209342-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209342
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209342
    reference: chr 1
allele count: 1
allele frequency: 1.050596738947722e-5
allele num: 95184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*46C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+145C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+145C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*46C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+145C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+145C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+145C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+145C>T
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11500
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10338
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6137
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

1-160209347-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209347
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209347
    reference: chr 1
allele count: 1
allele frequency: 1.043362130128125e-5
allele num: 95844
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+140A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+140A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+140A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+140A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+140A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+140A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*41A>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13808
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2659
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16751
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3454
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

1-160209348-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209348
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209348
    reference: chr 1
allele count: 3
allele frequency: 3.125976867771179e-5
allele num: 95970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+139A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+139A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+139A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+139A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+139A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*40A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*40A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+139A>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13491
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17794
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18435
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5476
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

1-160209350-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209350
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209350
    reference: chr 1
allele count: 4
allele frequency: 4.169446297531687e-5
allele num: 95936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+137C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*38C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*38C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+137C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+137C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+137C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+137C>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+137C>A
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19685
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20348
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4853
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5444
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

1-160209351-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209351
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209351
    reference: chr 1
allele count: 2
allele frequency: 2.077447232840286e-5
allele num: 96272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*37C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+136C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+136C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+136C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+136C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+136C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*37C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+136C>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8896
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

1-160209353-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209353
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209353
    reference: chr 1
allele count: 1
allele frequency: 1.033613097945177e-5
allele num: 96748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*35C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*35C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+134C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+134C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+134C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+134C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+134C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+134C>T
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 21426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4224
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8968
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3252
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

1-160209361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209361
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209361
    reference: chr 1
allele count: 972
allele frequency: 9.787336877718704e-3
allele num: 99312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+126C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+126C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+126C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+126C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+126C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+126C>T
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 8570
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 2.75e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 28118
  bin: 2.25e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 3.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 1.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 1.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 3.25e1
  variant carriers: 130
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 9.75e1
  variant carriers: 933
genotype quality: GenotypeQuality
  all individuals: 8416
  bin: 2.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 7.75e1
  variant carriers: 3
num of homozygotes: 19
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-160209364-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209364
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209364
    reference: chr 1
allele count: 1
allele frequency: 9.916503044366434e-6
allele num: 100842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*24C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+123C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*24C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+123C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+123C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+123C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+123C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+123C>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

1-160209375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209375
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209375
    reference: chr 1
allele count: 5
allele frequency: 4.660700969425801e-5
allele num: 107280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+112G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+112G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+112G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*13G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+112G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*13G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+112G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+112G>A
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34617
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10924
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5693
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5371
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

1-160209376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209376
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209376
    reference: chr 1
allele count: 4
allele frequency: 3.695969545210948e-5
allele num: 108226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*12C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+111C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+111C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+111C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*12C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+111C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+111C>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+111C>T
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11190
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5022
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

1-160209376-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209376
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209376
    reference: chr 1
allele count: 1
allele frequency: 9.239923863027369e-6
allele num: 108226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+111C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+111C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+111C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+111C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*12C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*12C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+111C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+111C>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39500
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5022
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

1-160209380-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209380
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209380
    reference: chr 1
allele count: 1
allele frequency: 9.055346276441612e-6
allele num: 110432
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+107A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*8A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+107A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+107A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+107A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*8A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+107A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+107A>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6011
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

1-160209386-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209386
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209386
    reference: chr 1
allele count: 5
allele frequency: 4.455374964357e-5
allele num: 112224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.*2A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+101A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+101A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.*2A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+101A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+101A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+101A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+101A>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37577
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11878
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6128
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

1-160209392-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209392
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209392
    reference: chr 1
allele count: 2
allele frequency: 1.757407472496573e-5
allele num: 113804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+95T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+95T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+95T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+95T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.818T>C
  hgvsp: ENSP00000476351.1:p.Leu273Ser
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+95T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.818T>C
  hgvsp: ENSP00000477464.1:p.Leu273Ser
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+95T>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6257
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu273Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

1-160209399-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209399
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209399
    reference: chr 1
allele count: 1
allele frequency: 8.686738824510502e-6
allele num: 115118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.811G>C
  hgvsp: ENSP00000476351.1:p.Glu271Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.811G>C
  hgvsp: ENSP00000477464.1:p.Glu271Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+88G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+88G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+88G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+88G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+88G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+88G>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38694
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2371
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu271Gln
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

1-160209403-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209403
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209403
    reference: chr 1
allele count: 4
allele frequency: 3.456798658762121e-5
allele num: 115714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+84T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+84T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.807T>C
  hgvsp: ENST00000475733.1:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+84T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+84T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.807T>C
  hgvsp: ENST00000610139.1:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+84T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+84T>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp269Asp
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

1-160209405-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209405
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209405
    reference: chr 1
allele count: 1
allele frequency: 8.625597322614591e-6
allele num: 115934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.805G>C
  hgvsp: ENSP00000476351.1:p.Asp269His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+82G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+82G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.805G>C
  hgvsp: ENSP00000477464.1:p.Asp269His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+82G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+82G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+82G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+82G>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44974
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6429
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp269His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-160209406-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209406
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209406
    reference: chr 1
allele count: 1
allele frequency: 8.611335962661248e-6
allele num: 116126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+81T>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+81T>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+81T>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+81T>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+81T>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.804T>G
  hgvsp: ENST00000475733.1:c.804T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.804T>G
  hgvsp: ENST00000610139.1:c.804T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+81T>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala268Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-160209442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209442
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209442
    reference: chr 1
allele count: 2
allele frequency: 1.691274713751755e-5
allele num: 118254
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+45G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+45G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.768G>A
  hgvsp: ENST00000475733.1:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+45G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+45G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.768G>A
  hgvsp: ENST00000610139.1:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+45G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+45G>A
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu256Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-160209444-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209444
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209444
    reference: chr 1
allele count: 203
allele frequency: 1.715106454883407e-3
allele num: 118360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+43G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+43G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+43G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.766G>C
  hgvsp: ENSP00000477464.1:p.Glu256Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+43G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+43G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+43G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.766G>C
  hgvsp: ENSP00000476351.1:p.Glu256Gln
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39539
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu256Gln
num of homozygotes: 2
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

1-160209444-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209444
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209444
    reference: chr 1
allele count: 1
allele frequency: 8.448800270361608e-6
allele num: 118360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.766G>A
  hgvsp: ENSP00000477464.1:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+43G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+43G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.766G>A
  hgvsp: ENSP00000476351.1:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+43G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+43G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+43G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+43G>A
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6604
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu256Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

1-160209445-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209445
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209445
    reference: chr 1
allele count: 3
allele frequency: 2.532842524737429e-5
allele num: 118444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+42T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.765T>C
  hgvsp: ENST00000475733.1:c.765T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+42T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+42T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.765T>C
  hgvsp: ENST00000610139.1:c.765T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+42T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+42T>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+42T>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46242
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His255His
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

1-160209449-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209449
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209449
    reference: chr 1
allele count: 2
allele frequency: 1.685601591207902e-5
allele num: 118652
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+38G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+38G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+38G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+38G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.761G>A
  hgvsp: ENSP00000476351.1:p.Arg254Lys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+38G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.761G>A
  hgvsp: ENSP00000477464.1:p.Arg254Lys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+38G>A
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg254Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

1-160209450-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209450
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209450
    reference: chr 1
allele count: 1
allele frequency: 8.425025696328374e-6
allele num: 118694
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+37A>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+37A>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+37A>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.760A>C
  hgvsp: ENST00000475733.1:c.760A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+37A>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.760A>C
  hgvsp: ENST00000610139.1:c.760A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+37A>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+37A>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg254Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

1-160209451-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209451
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209451
    reference: chr 1
allele count: 2
allele frequency: 1.683870207284422e-5
allele num: 118774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+36C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.759C>G
  hgvsp: ENSP00000476351.1:p.Ile253Met
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.759C>G
  hgvsp: ENSP00000477464.1:p.Ile253Met
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+36C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+36C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+36C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+36C>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+36C>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile253Met
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

1-160209457-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209457
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209457
    reference: chr 1
allele count: 43
allele frequency: 3.61126041386724e-4
allele num: 119072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+30G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+30G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+30G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.753G>C
  hgvsp: ENSP00000477464.1:p.Glu251Asp
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.753G>C
  hgvsp: ENSP00000476351.1:p.Glu251Asp
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+30G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+30G>C
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+30G>C
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39743
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu251Asp
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

1-160209462-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209462
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209462
    reference: chr 1
allele count: 5
allele frequency: 4.191958147489856e-5
allele num: 119276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+25A>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+25A>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+25A>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.748A>T
  hgvsp: ENSP00000477464.1:p.Thr250Ser
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+25A>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+25A>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+25A>T
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.748A>T
  hgvsp: ENSP00000476351.1:p.Thr250Ser
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr250Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

1-160209469-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209469
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209469
    reference: chr 1
allele count: 1
allele frequency: 8.363581620193032e-6
allele num: 119566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+18A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+18A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.741A>G
  hgvsp: ENSP00000476351.1:p.Ile247Met
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+18A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.741A>G
  hgvsp: ENSP00000477464.1:p.Ile247Met
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+18A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+18A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+18A>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13695
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile247Met
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

1-160209471-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209471
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209471
    reference: chr 1
allele count: 1
allele frequency: 8.358967500334358e-6
allele num: 119632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+16A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+16A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+16A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.739A>G
  hgvsp: ENSP00000476351.1:p.Ile247Val
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+16A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.739A>G
  hgvsp: ENSP00000477464.1:p.Ile247Val
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+16A>G
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+16A>G
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46641
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile247Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-160209476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209476
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209476
    reference: chr 1
allele count: 3
allele frequency: 2.501626056937009e-5
allele num: 119922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.723+11G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.723+11G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.723+11G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.734G>A
  hgvsp: ENSP00000477464.1:p.Gly245Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.734G>A
  hgvsp: ENSP00000476351.1:p.Gly245Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1185+11G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.723+11G>A
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1185+11G>A
  variant of: http://identifiers.org/hgnc/24891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46820
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6715
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly245Glu
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-160209500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209500
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209500
    reference: chr 1
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.710G>A
  hgvsp: ENSP00000357053.1:p.Ser237Asn
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1172G>A
  hgvsp: ENSP00000451235.1:p.Ser391Asn
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.710G>A
  hgvsp: ENSP00000477464.1:p.Ser237Asn
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.710G>A
  hgvsp: ENSP00000476407.1:p.Ser237Asn
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.710G>A
  hgvsp: ENSP00000357052.3:p.Ser237Asn
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.710G>A
  hgvsp: ENSP00000476351.1:p.Ser237Asn
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.710G>A
  hgvsp: ENSP00000318227.2:p.Ser237Asn
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1172G>A
  hgvsp: ENSP00000476284.1:p.Ser391Asn
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser237Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

1-160209520-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209520
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209520
    reference: chr 1
allele count: 1
allele frequency: 8.291048983517394e-6
allele num: 120612
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1152C>G
  hgvsp: ENSP00000451235.1:p.Asp384Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1152C>G
  hgvsp: ENSP00000476284.1:p.Asp384Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.690C>G
  hgvsp: ENSP00000357053.1:p.Asp230Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.690C>G
  hgvsp: ENSP00000357052.3:p.Asp230Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.690C>G
  hgvsp: ENSP00000477464.1:p.Asp230Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.690C>G
  hgvsp: ENSP00000318227.2:p.Asp230Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.690C>G
  hgvsp: ENSP00000476407.1:p.Asp230Glu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.690C>G
  hgvsp: ENSP00000476351.1:p.Asp230Glu
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp230Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-160209535-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209535
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209535
    reference: chr 1
allele count: 774
allele frequency: 6.873767783875952e-3
allele num: 112602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.675G>C
  hgvsp: ENST00000368074.1:c.675G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.675G>C
  hgvsp: ENST00000368073.3:c.675G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.675G>C
  hgvsp: ENST00000326837.2:c.675G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1137G>C
  hgvsp: ENST00000608310.1:c.1137G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.675G>C
  hgvsp: ENST00000610139.1:c.675G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.675G>C
  hgvsp: ENST00000461888.1:c.675G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.675G>C
  hgvsp: ENST00000475733.1:c.675G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1137G>C
  hgvsp: ENST00000556710.1:c.1137G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 3.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 13136
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 38026
  bin: 2.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 9.75e1
  variant carriers: 580
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 19
hgvs: p.Arg225Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

1-160209537-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209537
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209537
    reference: chr 1
allele count: 1
allele frequency: 8.337224037884346e-6
allele num: 119944
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1135C>A
  hgvsp: ENST00000556710.1:c.1135C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.673C>A
  hgvsp: ENST00000610139.1:c.673C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.673C>A
  hgvsp: ENST00000461888.1:c.673C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.673C>A
  hgvsp: ENST00000326837.2:c.673C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.673C>A
  hgvsp: ENST00000368073.3:c.673C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1135C>A
  hgvsp: ENST00000608310.1:c.1135C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.673C>A
  hgvsp: ENST00000475733.1:c.673C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.673C>A
  hgvsp: ENST00000368074.1:c.673C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg225Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-160209538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209538
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209538
    reference: chr 1
allele count: 1
allele frequency: 8.326810664979099e-6
allele num: 120094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.672G>A
  hgvsp: ENST00000368074.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.672G>A
  hgvsp: ENST00000461888.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.672G>A
  hgvsp: ENST00000475733.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1134G>A
  hgvsp: ENST00000556710.1:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.672G>A
  hgvsp: ENST00000610139.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.672G>A
  hgvsp: ENST00000326837.2:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.672G>A
  hgvsp: ENST00000368073.3:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1134G>A
  hgvsp: ENST00000608310.1:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6678
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg224Arg
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

1-160209539-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209539
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209539
    reference: chr 1
allele count: 2
allele frequency: 1.66536213299582e-5
allele num: 120094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.671G>A
  hgvsp: ENSP00000357053.1:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.671G>A
  hgvsp: ENSP00000357052.3:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.671G>A
  hgvsp: ENSP00000476407.1:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.671G>A
  hgvsp: ENSP00000476351.1:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.671G>A
  hgvsp: ENSP00000477464.1:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1133G>A
  hgvsp: ENSP00000451235.1:p.Arg378Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.671G>A
  hgvsp: ENSP00000318227.2:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1133G>A
  hgvsp: ENSP00000476284.1:p.Arg378Gln
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6679
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg224Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

1-160209541-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209541
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209541
    reference: chr 1
allele count: 2
allele frequency: 1.665417603464068e-5
allele num: 120090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.669A>C
  hgvsp: ENST00000326837.2:c.669A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1131A>C
  hgvsp: ENST00000608310.1:c.1131A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.669A>C
  hgvsp: ENST00000475733.1:c.669A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.669A>C
  hgvsp: ENST00000610139.1:c.669A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.669A>C
  hgvsp: ENST00000368073.3:c.669A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.669A>C
  hgvsp: ENST00000461888.1:c.669A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.669A>C
  hgvsp: ENST00000368074.1:c.669A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1131A>C
  hgvsp: ENST00000556710.1:c.1131A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45882
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val223Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-160209542-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209542
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209542
    reference: chr 1
allele count: 1
allele frequency: 8.329862557267805e-6
allele num: 120050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.668T>G
  hgvsp: ENSP00000476351.1:p.Val223Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.668T>G
  hgvsp: ENSP00000357053.1:p.Val223Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.668T>G
  hgvsp: ENSP00000477464.1:p.Val223Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.668T>G
  hgvsp: ENSP00000318227.2:p.Val223Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.668T>G
  hgvsp: ENSP00000476407.1:p.Val223Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1130T>G
  hgvsp: ENSP00000451235.1:p.Val377Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1130T>G
  hgvsp: ENSP00000476284.1:p.Val377Gly
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.668T>G
  hgvsp: ENSP00000357052.3:p.Val223Gly
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13727
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6702
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45856
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val223Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

1-160209542-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209542
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209542
    reference: chr 1
allele count: 1
allele frequency: 8.329862557267805e-6
allele num: 120050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.668T>C
  hgvsp: ENSP00000318227.2:p.Val223Ala
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.668T>C
  hgvsp: ENSP00000477464.1:p.Val223Ala
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.668T>C
  hgvsp: ENSP00000476407.1:p.Val223Ala
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.668T>C
  hgvsp: ENSP00000357053.1:p.Val223Ala
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.668T>C
  hgvsp: ENSP00000357052.3:p.Val223Ala
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1130T>C
  hgvsp: ENSP00000476284.1:p.Val377Ala
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.668T>C
  hgvsp: ENSP00000476351.1:p.Val223Ala
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1130T>C
  hgvsp: ENSP00000451235.1:p.Val377Ala
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45856
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val223Ala
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-160209543-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209543
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209543
    reference: chr 1
allele count: 2
allele frequency: 1.664946222237022e-5
allele num: 120124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.667G>T
  hgvsp: ENSP00000477464.1:p.Val223Leu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.667G>T
  hgvsp: ENSP00000476351.1:p.Val223Leu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.667G>T
  hgvsp: ENSP00000357053.1:p.Val223Leu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.667G>T
  hgvsp: ENSP00000357052.3:p.Val223Leu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.667G>T
  hgvsp: ENSP00000318227.2:p.Val223Leu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.667G>T
  hgvsp: ENSP00000476407.1:p.Val223Leu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1129G>T
  hgvsp: ENSP00000451235.1:p.Val377Leu
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1129G>T
  hgvsp: ENSP00000476284.1:p.Val377Leu
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val223Leu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

1-160209553-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209553
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209553
    reference: chr 1
allele count: 1
allele frequency: 8.32126749546491e-6
allele num: 120174
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.657G>A
  hgvsp: ENST00000368073.3:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.657G>A
  hgvsp: ENST00000475733.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.657G>A
  hgvsp: ENST00000326837.2:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1119G>A
  hgvsp: ENST00000608310.1:c.1119G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.657G>A
  hgvsp: ENST00000610139.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1119G>A
  hgvsp: ENST00000556710.1:c.1119G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.657G>A
  hgvsp: ENST00000368074.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.657G>A
  hgvsp: ENST00000461888.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val219Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

1-160209568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209568
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209568
    reference: chr 1
allele count: 22
allele frequency: 1.8297957282587e-4
allele num: 120232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.642C>T
  hgvsp: ENST00000368074.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.642C>T
  hgvsp: ENST00000475733.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.642C>T
  hgvsp: ENST00000610139.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1104C>T
  hgvsp: ENST00000556710.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.642C>T
  hgvsp: ENST00000326837.2:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.642C>T
  hgvsp: ENST00000368073.3:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1104C>T
  hgvsp: ENST00000608310.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.642C>T
  hgvsp: ENST00000461888.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38194
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp214Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

1-160209574-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209574
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209574
    reference: chr 1
allele count: 8
allele frequency: 6.697362913352868e-5
allele num: 119450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.636C>T
  hgvsp: ENST00000326837.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.636C>T
  hgvsp: ENST00000610139.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.636C>T
  hgvsp: ENST00000368073.3:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.636C>T
  hgvsp: ENST00000461888.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1098C>T
  hgvsp: ENST00000608310.1:c.1098C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.636C>T
  hgvsp: ENST00000368074.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.636C>T
  hgvsp: ENST00000475733.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.636C>T
  hgvsp: ENST00000447377.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1098C>T
  hgvsp: ENST00000556710.1:c.1098C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38194
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser212Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

1-160209574-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209574
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209574
    reference: chr 1
allele count: 16
allele frequency: 1.339472582670574e-4
allele num: 119450
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.636C>G
  hgvsp: ENSP00000413688.1:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.636C>G
  hgvsp: ENSP00000357052.3:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.636C>G
  hgvsp: ENSP00000318227.2:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.636C>G
  hgvsp: ENSP00000357053.1:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.636C>G
  hgvsp: ENSP00000477464.1:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.636C>G
  hgvsp: ENSP00000476351.1:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.636C>G
  hgvsp: ENSP00000476407.1:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1098C>G
  hgvsp: ENSP00000451235.1:p.Ser366Arg
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1098C>G
  hgvsp: ENSP00000476284.1:p.Ser366Arg
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13991
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38194
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser212Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

1-160209581-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209581
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209581
    reference: chr 1
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.629G>C
  hgvsp: ENSP00000476351.1:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1091G>C
  hgvsp: ENSP00000476284.1:p.Ser364Thr
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.629G>C
  hgvsp: ENSP00000357052.3:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1091G>C
  hgvsp: ENSP00000451235.1:p.Ser364Thr
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.629G>C
  hgvsp: ENSP00000413688.1:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.629G>C
  hgvsp: ENSP00000318227.2:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.629G>C
  hgvsp: ENSP00000357053.1:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.629G>C
  hgvsp: ENSP00000476407.1:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.629G>C
  hgvsp: ENSP00000477464.1:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser210Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/1-160209586-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209586
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209586
    reference: chr 1
allele count: 2
allele frequency: 1.653165812530997e-5
allele num: 120980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.624G>T
  hgvsp: ENST00000368074.1:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.624G>T
  hgvsp: ENST00000610139.1:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.624G>T
  hgvsp: ENST00000461888.1:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1086G>T
  hgvsp: ENST00000556710.1:c.1086G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.624G>T
  hgvsp: ENST00000475733.1:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.624G>T
  hgvsp: ENST00000326837.2:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1086G>T
  hgvsp: ENST00000608310.1:c.1086G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.624G>T
  hgvsp: ENST00000447377.1:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.624G>T
  hgvsp: ENST00000368073.3:c.624G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu208Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

1-160209588-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209588
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209588
    reference: chr 1
allele count: 1
allele frequency: 8.263097008758882e-6
allele num: 121020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.622C>T
  hgvsp: ENST00000610139.1:c.622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.622C>T
  hgvsp: ENST00000368074.1:c.622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.622C>T
  hgvsp: ENST00000368073.3:c.622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.622C>T
  hgvsp: ENST00000447377.1:c.622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1084C>T
  hgvsp: ENST00000608310.1:c.1084C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.622C>T
  hgvsp: ENST00000461888.1:c.622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.622C>T
  hgvsp: ENST00000326837.2:c.622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.622C>T
  hgvsp: ENST00000475733.1:c.622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1084C>T
  hgvsp: ENST00000556710.1:c.1084C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46507
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6770
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu208Leu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/1-160209589-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209589
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209589
    reference: chr 1
allele count: 1
allele frequency: 8.259275166011431e-6
allele num: 121076
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1083G>T
  hgvsp: ENSP00000451235.1:p.Trp361Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.621G>T
  hgvsp: ENSP00000477464.1:p.Trp207Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.621G>T
  hgvsp: ENSP00000476407.1:p.Trp207Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.621G>T
  hgvsp: ENSP00000318227.2:p.Trp207Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.621G>T
  hgvsp: ENSP00000357053.1:p.Trp207Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.621G>T
  hgvsp: ENSP00000357052.3:p.Trp207Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1083G>T
  hgvsp: ENSP00000476284.1:p.Trp361Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.621G>T
  hgvsp: ENSP00000413688.1:p.Trp207Cys
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.621G>T
  hgvsp: ENSP00000476351.1:p.Trp207Cys
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Trp207Cys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

1-160209592-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209592
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209592
    reference: chr 1
allele count: 5
allele frequency: 4.124731892426992e-5
allele num: 121220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.618C>G
  hgvsp: ENST00000368074.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1080C>G
  hgvsp: ENST00000556710.1:c.1080C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.618C>G
  hgvsp: ENST00000461888.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.618C>G
  hgvsp: ENST00000475733.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.618C>G
  hgvsp: ENST00000326837.2:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.618C>G
  hgvsp: ENST00000368073.3:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.618C>G
  hgvsp: ENST00000447377.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1080C>G
  hgvsp: ENST00000608310.1:c.1080C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.618C>G
  hgvsp: ENST00000610139.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr206Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

1-160209598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209598
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209598
    reference: chr 1
allele count: 169
allele frequency: 1.393239901071723e-3
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.612C>T
  hgvsp: ENST00000610139.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.612C>T
  hgvsp: ENST00000475733.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.612C>T
  hgvsp: ENST00000461888.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.612C>T
  hgvsp: ENST00000368073.3:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.612C>T
  hgvsp: ENST00000326837.2:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1074C>T
  hgvsp: ENST00000608310.1:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.612C>T
  hgvsp: ENST00000447377.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1074C>T
  hgvsp: ENST00000556710.1:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.612C>T
  hgvsp: ENST00000368074.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14779
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 38443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg204Arg
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-160209599-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 160209599
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 160209599
    reference: chr 1
allele count: 3
allele frequency: 2.473003050037095e-5
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258465
  ensembl protein: ENSP00000451235
  ensembl transcript: ENST00000556710
  gene symbol: DCAF8
  hgvsc: ENST00000556710.1:c.1073G>A
  hgvsp: ENSP00000451235.1:p.Arg358His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476351
  ensembl transcript: ENST00000475733
  gene symbol: DCAF8
  hgvsc: ENST00000475733.1:c.611G>A
  hgvsp: ENSP00000476351.1:p.Arg204His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000477464
  ensembl transcript: ENST00000610139
  gene symbol: DCAF8
  hgvsc: ENST00000610139.1:c.611G>A
  hgvsp: ENSP00000477464.1:p.Arg204His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476284
  ensembl transcript: ENST00000608310
  gene symbol: DCAF8
  hgvsc: ENST00000608310.1:c.1073G>A
  hgvsp: ENSP00000476284.1:p.Arg358His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000413688
  ensembl transcript: ENST00000447377
  gene symbol: DCAF8
  hgvsc: ENST00000447377.1:c.611G>A
  hgvsp: ENSP00000413688.1:p.Arg204His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000476407
  ensembl transcript: ENST00000461888
  gene symbol: DCAF8
  hgvsc: ENST00000461888.1:c.611G>A
  hgvsp: ENSP00000476407.1:p.Arg204His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357052
  ensembl transcript: ENST00000368073
  gene symbol: DCAF8
  hgvsc: ENST00000368073.3:c.611G>A
  hgvsp: ENSP00000357052.3:p.Arg204His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000357053
  ensembl transcript: ENST00000368074
  gene symbol: DCAF8
  hgvsc: ENST00000368074.1:c.611G>A
  hgvsp: ENSP00000357053.1:p.Arg204His
  variant of: http://identifiers.org/hgnc/24891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132716
  ensembl protein: ENSP00000318227
  ensembl transcript: ENST00000326837
  gene symbol: DCAF8
  hgvsc: ENST00000326837.2:c.611G>A
  hgvsp: ENSP00000318227.2:p.Arg204His
  variant of: http://identifiers.org/hgnc/24891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg204His
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 623
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41533
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 387
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.174364040503828e-5
allele num: 16196
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.158e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

DP
type: SiteQuality
SIO_000300: 1.578441e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.487e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.631e0

MQRankSum
type: SiteQuality
SIO_000300: -9.21e-1

QD
type: SiteQuality
SIO_000300: 5.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

GenotypeQuality
all individuals: 729
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40643
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6627
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.176652254478072e-5
allele num: 16190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.876e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.905e0

QD
type: SiteQuality
SIO_000300: 1.091e1

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

DP
type: SiteQuality
SIO_000300: 1.574654e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40110
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2299
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6360
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.098277357789069e-4
allele num: 16138
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.563084e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.081e0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1860
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 40677
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 344
bin: 9.25e1
variant carriers: 7

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

GenotypeQuality
all individuals: 667
bin: 8.25e1
variant carriers: 2

Latino
type: Population
allele count: 306
allele frequency: 2.704135737009544e-2
allele num: 11316
num of homozygotes: 7

South Asian
type: Population
allele count: 16
allele frequency: 9.924327006574866e-4
allele num: 16122
num of homozygotes: 0

African
type: Population
allele count: 527
allele frequency: 5.164641317130537e-2
allele num: 10204
num of homozygotes: 16

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.57825770444067e-4
allele num: 65936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

East Asian
type: Population
allele count: 203
allele frequency: 2.361563517915309e-2
allele num: 8596
num of homozygotes: 4

Other
type: Population
allele count: 4
allele frequency: 4.484304932735426e-3
allele num: 892
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

FS
type: SiteQuality
SIO_000300: 5.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.59e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.453e1

DP
type: SiteQuality
SIO_000300: 1.56256e6

GenotypeQuality
all individuals: 2210
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 719
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 337
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2001
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522301720200944e-5
allele num: 65690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.611e0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.306e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

QD
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 1.539498e6

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 41560
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.879470460383324e-5
allele num: 10122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045345189877273e-5
allele num: 65674
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166861143523921e-4
allele num: 8570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.227425582264292e-5
allele num: 16058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11256
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

FS
type: SiteQuality
SIO_000300: 3.256e0

QD
type: SiteQuality
SIO_000300: 1.205e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

DP
type: SiteQuality
SIO_000300: 1.53804e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

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

GenotypeQuality
all individuals: 1533
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5968
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 41523
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16048
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.895111814763506e-5
allele num: 10106
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.047201145747631e-5
allele num: 65634
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

DP
type: SiteQuality
SIO_000300: 1.533852e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.553e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 41101
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545499505440158e-5
allele num: 64704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.634e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.15e-1

DP
type: SiteQuality
SIO_000300: 1.49627e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

VQSLOD
type: SiteQuality
SIO_000300: -2.776e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

GenotypeQuality
all individuals: 4235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41330
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547748026621266e-5
allele num: 64610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.913e0

VQSLOD
type: SiteQuality
SIO_000300: -7.294e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.099e0

DP
type: SiteQuality
SIO_000300: 1.490776e6

QD
type: SiteQuality
SIO_000300: 1.104e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.84e-1

GenotypeQuality
all individuals: 33022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.076889941847943e-4
allele num: 9286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8086
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.823e0

DP
type: SiteQuality
SIO_000300: 1.368412e6

MQ
type: SiteQuality
SIO_000300: 5.884e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 4.72e0

MQRankSum
type: SiteQuality
SIO_000300: -1.347e0

VQSLOD
type: SiteQuality
SIO_000300: -3.115e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

GenotypeQuality
all individuals: 927
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 940
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.1654395842356e-4
allele num: 9236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 4.745e0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.177e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

DP
type: SiteQuality
SIO_000300: 1.350537e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2795
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30275
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 465
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62030
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.261578604044357e-4
allele num: 9198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 8.149999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

DP
type: SiteQuality
SIO_000300: 1.332895e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

QD
type: SiteQuality
SIO_000300: 8.74e0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27218
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7892
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627286337303912e-5
allele num: 61452
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.416e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 1.271128e6

QD
type: SiteQuality
SIO_000300: 1.295e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.15e-1

GenotypeQuality
all individuals: 816
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2700
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1049
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5056
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.123521869212138e-5
allele num: 14038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.232e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.75e0

FS
type: SiteQuality
SIO_000300: 5.971e0

DP
type: SiteQuality
SIO_000300: 1.239582e6

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.322e-1

GenotypeQuality
all individuals: 682
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19696
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6784
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.132246376811594e-4
allele num: 8832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7718
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.083e1

DP
type: SiteQuality
SIO_000300: 1.16067e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

QD
type: SiteQuality
SIO_000300: 2.027e1

MQRankSum
type: SiteQuality
SIO_000300: -1.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7738
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5346
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 969
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6244
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.431708991077557e-4
allele num: 8742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7672
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.613e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.573e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.125886e6

QD
type: SiteQuality
SIO_000300: 6.9e0

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5615
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13993
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5650
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 304
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.812319538017325e-4
allele num: 6234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13700
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.01002004008016e-5
allele num: 59880
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.980329823167097e-4
allele num: 10066
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.506265664160401e-3
allele num: 798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7638
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.383e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

FS
type: SiteQuality
SIO_000300: 5.887e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

DP
type: SiteQuality
SIO_000300: 1.093431e6

GenotypeQuality
all individuals: 1125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10902
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59230
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.166861143523921e-4
allele num: 8570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13486
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

QD
type: SiteQuality
SIO_000300: 1.517e1

DP
type: SiteQuality
SIO_000300: 1.067352e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

FS
type: SiteQuality
SIO_000300: 1.505e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14624
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2514
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7194
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.504890895410083e-4
allele num: 13290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58818
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.047878e6

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

MQ
type: SiteQuality
SIO_000300: 6.06e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

FS
type: SiteQuality
SIO_000300: 1.954e0

QD
type: SiteQuality
SIO_000300: 1.102e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

GenotypeQuality
all individuals: 1327
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 987
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1191
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5918
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7364
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.478781988986071e-4
allele num: 6174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.195681880295163e-4
allele num: 58544
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

FS
type: SiteQuality
SIO_000300: 1.134e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.294e1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.775e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.64e-1

DP
type: SiteQuality
SIO_000300: 1.041489e6

GenotypeQuality
all individuals: 603
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5586
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3279
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5949
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7277
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1061
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3113
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.852881230313137e-5
allele num: 53970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.355e0

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-2

QD
type: SiteQuality
SIO_000300: 1.434e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

DP
type: SiteQuality
SIO_000300: 1.007065e6

GenotypeQuality
all individuals: 5752
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3505
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5760
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8541
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.596928982725528e-5
allele num: 10420
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.157e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

QD
type: SiteQuality
SIO_000300: 4.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.62e0

DP
type: SiteQuality
SIO_000300: 1.039228e6

GenotypeQuality
all individuals: 843
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5677
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2824
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8770
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3489
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2381
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.875766871165644e-4
allele num: 10432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.049543e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

QD
type: SiteQuality
SIO_000300: 1.014e1

GenotypeQuality
all individuals: 8930
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2172
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2201
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3409
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 9.75e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.832886163280951e-4
allele num: 10436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54310
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

QD
type: SiteQuality
SIO_000300: 1.426e1

DP
type: SiteQuality
SIO_000300: 1.071553e6

GenotypeQuality
all individuals: 1864
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5341
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3379
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4677
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1081
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54476
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.518370454978108e-5
allele num: 10506
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.384274640088594e-4
allele num: 7224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7696
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

DP
type: SiteQuality
SIO_000300: 1.078742e6

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.156e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

QD
type: SiteQuality
SIO_000300: 1.903e1

GenotypeQuality
all individuals: 660
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3922
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5071
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.380834023750345e-4
allele num: 7242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9874
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.575e0

QD
type: SiteQuality
SIO_000300: 1.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.272e0

DP
type: SiteQuality
SIO_000300: 1.094262e6

GenotypeQuality
all individuals: 401
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3134
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 29302
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 267
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1736
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 614
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 721
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 4524
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1211
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 662
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 3

Other
type: Population
allele count: 4
allele frequency: 5.46448087431694e-3
allele num: 732
num of homozygotes: 0

East Asian
type: Population
allele count: 194
allele frequency: 2.610333692142088e-2
allele num: 7432
num of homozygotes: 4

South Asian
type: Population
allele count: 15
allele frequency: 1.363636363636364e-3
allele num: 11000
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5952
num of homozygotes: 0

Latino
type: Population
allele count: 297
allele frequency: 2.907204385277995e-2
allele num: 10216
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.853575887283753e-4
allele num: 56070
num of homozygotes: 0

African
type: Population
allele count: 446
allele frequency: 5.638432364096081e-2
allele num: 7910
num of homozygotes: 10

QD
type: SiteQuality
SIO_000300: 1.528e1

VQSLOD
type: SiteQuality
SIO_000300: 5.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.43e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.756e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

DP
type: SiteQuality
SIO_000300: 1.189006e6

GenotypeQuality
all individuals: 886
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4939
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10474
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.25093820365274e-4
allele num: 7994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56840
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.222182e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.71e0

QD
type: SiteQuality
SIO_000300: 1.759e1

GenotypeQuality
all individuals: 130
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38752
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.664004259850905e-5
allele num: 60096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.203079884504331e-4
allele num: 8312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11086
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 2.366677185231934e-4
allele num: 12676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

MQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

FS
type: SiteQuality
SIO_000300: 2.163e0

DP
type: SiteQuality
SIO_000300: 1.321228e6

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 5780
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1225
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39500
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.609166914510426e-5
allele num: 60522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

QD
type: SiteQuality
SIO_000300: 1.267e1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

FS
type: SiteQuality
SIO_000300: 6.837e0

DP
type: SiteQuality
SIO_000300: 1.33504e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5780
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.975049362771496e-5
allele num: 11142
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.837e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

DP
type: SiteQuality
SIO_000300: 1.33504e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4261
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627233377811046e-5
allele num: 61454
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.94e-1

FS
type: SiteQuality
SIO_000300: 3.045e0

DP
type: SiteQuality
SIO_000300: 1.358554e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.49e0

QD
type: SiteQuality
SIO_000300: 1.424e1

GenotypeQuality
all individuals: 132
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42693
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 872
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.219160442956477e-5
allele num: 62128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.379881330205602e-4
allele num: 14494
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.805917576611483e-5
allele num: 11356
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.479e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

DP
type: SiteQuality
SIO_000300: 1.378943e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 1616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43693
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.186336986999745e-5
allele num: 62768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15194
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.392e1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.213e0

FS
type: SiteQuality
SIO_000300: 4.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.396808e6

VQSLOD
type: SiteQuality
SIO_000300: -6.13e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
all individuals: 235
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1644
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44427
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.180916391119509e-4
allele num: 8468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.411762e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.775e1

GenotypeQuality
all individuals: 1653
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6416
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.137656427758817e-4
allele num: 8790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.72232716282584e-5
allele num: 63528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.48e-1

DP
type: SiteQuality
SIO_000300: 1.418413e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.15e0

FS
type: SiteQuality
SIO_000300: 8.44e-1

QD
type: SiteQuality
SIO_000300: 1.665e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeQuality
all individuals: 899
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1647
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 518
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63626
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.713837574067619e-5
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.449e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.561e0

FS
type: SiteQuality
SIO_000300: 6.632e0

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 1.421611e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.569957297161517e-5
allele num: 63696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

DP
type: SiteQuality
SIO_000300: 1.422774e6

FS
type: SiteQuality
SIO_000300: 2.017e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

QD
type: SiteQuality
SIO_000300: 1.625e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 3.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.76e0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46164
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6628
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 903
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.082329007798292e-5
allele num: 64886
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: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.446496e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.354e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.621e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.54e-1

QD
type: SiteQuality
SIO_000300: 1.325e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.052e0

GenotypeQuality
all individuals: 1672
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6604
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 46104
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 9.75e1
variant carriers: 198

GenotypeQuality
all individuals: 895
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 344
bin: 9.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 188
allele frequency: 2.026735661923243e-2
allele num: 9276
num of homozygotes: 2

Latino
type: Population
allele count: 14
allele frequency: 1.211072664359861e-3
allele num: 11560
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: 8594
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

QD
type: SiteQuality
SIO_000300: 1.431e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

DP
type: SiteQuality
SIO_000300: 1.461073e6

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1354
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1672
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64922
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.431e1

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 1.461073e6

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6648
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1686
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1733
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.22234156820623e-4
allele num: 9310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 64972
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.450282e6

MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: 7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.601e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

QD
type: SiteQuality
SIO_000300: 1.247e1

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

GenotypeQuality
all individuals: 336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6660
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730103806228374e-4
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65094
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.427e0

VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

DP
type: SiteQuality
SIO_000300: 1.452072e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

QD
type: SiteQuality
SIO_000300: 1.285e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.225e0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46323
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1267
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65120
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9404
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: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: -1.029e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

FS
type: SiteQuality
SIO_000300: 6.492e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

QD
type: SiteQuality
SIO_000300: 1.223e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.979e0

DP
type: SiteQuality
SIO_000300: 1.452503e6

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6669
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1691
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 906
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.059322033898305e-4
allele num: 9440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534636751480924e-5
allele num: 65162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
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: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.09e-1

DP
type: SiteQuality
SIO_000300: 1.453618e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.355e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.33e-1

FS
type: SiteQuality
SIO_000300: 3.832e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

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

GenotypeQuality
all individuals: 907
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 9.75e1
variant carriers: 42

GenotypeQuality
all individuals: 6679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 5.355776587605203e-4
allele num: 65350
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9534
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.209555488358028e-3
allele num: 6614
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.459641e6

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

FS
type: SiteQuality
SIO_000300: 5.92e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.65e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.13e-1

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6690
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 9.75e1
variant carriers: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65478
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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: 5
allele frequency: 5.206164098292378e-4
allele num: 9604
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.458724e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 2.667e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523414886810274e-5
allele num: 65642
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.846e1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.453e1

FS
type: SiteQuality
SIO_000300: 2.905e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

VQSLOD
type: SiteQuality
SIO_000300: -3.98e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.460676e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 903
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 7.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.772e0

QD
type: SiteQuality
SIO_000300: 1.209e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 1.461546e6

VQSLOD
type: SiteQuality
SIO_000300: 1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.533e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.97e0

GenotypeQuality
all individuals: 1695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 832
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 8.25e1
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: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.037298019681691e-5
allele num: 65848
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.048e0

MQRankSum
type: SiteQuality
SIO_000300: -5.71e-1

FS
type: SiteQuality
SIO_000300: 3.384e0

DP
type: SiteQuality
SIO_000300: 1.464518e6

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.172e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
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: 11574
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.844457570387872e-5
allele num: 10158
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 1.473603e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.107e0

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-1

QD
type: SiteQuality
SIO_000300: 1.241e1

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6740
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46678
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.699e0

FS
type: SiteQuality
SIO_000300: 1.5842e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.472554e6

MQRankSum
type: SiteQuality
SIO_000300: -1.076e0

QD
type: SiteQuality
SIO_000300: 2.371e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: -1.796e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.257e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
all individuals: 1392
bin: 7.75e1
variant carriers: 20

GenotypeQuality
all individuals: 6002
bin: 6.75e1
variant carriers: 13

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 12

GenotypeQuality
all individuals: 332
bin: 2.25e1
variant carriers: 12

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 14

GenotypeQuality
all individuals: 44067
bin: 6.25e1
variant carriers: 12

GenotypeQuality
all individuals: 3750
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 12

GenotypeQuality
all individuals: 726
bin: 8.25e1
variant carriers: 16

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 15

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1483
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 255
bin: 9.25e1
variant carriers: 15

European (Finnish)
type: Population
allele count: 148
allele frequency: 2.675343456254519e-2
allele num: 5532
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 1.492537313432836e-3
allele num: 11390
num of homozygotes: 0

East Asian
type: Population
allele count: 26
allele frequency: 3.084954912197437e-3
allele num: 8428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 469
allele frequency: 7.650148435715917e-3
allele num: 61306
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 1.133501259445844e-2
allele num: 794
num of homozygotes: 0

African
type: Population
allele count: 102
allele frequency: 1.177829099307159e-2
allele num: 8660
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819063788503517e-4
allele num: 16492
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.82e-2

FS
type: SiteQuality
SIO_000300: 2.47765e2

VQSLOD
type: SiteQuality
SIO_000300: -2.788e2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.625e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.51e-1

MQ
type: SiteQuality
SIO_000300: 5.849e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.603064e6

QD
type: SiteQuality
SIO_000300: 2.69e0

GenotypeQuality
all individuals: 482
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6655
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45488
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518787400139728e-5
allele num: 65842
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.501465e6

FS
type: SiteQuality
SIO_000300: 3.245e0

QD
type: SiteQuality
SIO_000300: 2.725e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.435e0

VQSLOD
type: SiteQuality
SIO_000300: -2.878e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1719
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45664
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517036317849449e-5
allele num: 65918
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

FS
type: SiteQuality
SIO_000300: 3.34e0

VQSLOD
type: SiteQuality
SIO_000300: -2.918e0

QD
type: SiteQuality
SIO_000300: 2.727e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.321e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.185e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.500146e6

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 1
allele frequency: 1.001803245842517e-4
allele num: 9982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65914
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.81e-1

DP
type: SiteQuality
SIO_000300: 1.500496e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQ
type: SiteQuality
SIO_000300: 5.987e1

QD
type: SiteQuality
SIO_000300: 1.365e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

MQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

FS
type: SiteQuality
SIO_000300: 1.0551e1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-1

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6704
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1705
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.521606816798539e-4
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517082347229808e-5
allele num: 65916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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: 16510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.500668e6

MQ
type: SiteQuality
SIO_000300: 5.73e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.597e0

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

VQSLOD
type: SiteQuality
SIO_000300: -2.808e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 6.6e-1

GenotypeQuality
all individuals: 1447
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516990291262136e-5
allele num: 65920
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

MQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.558e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

DP
type: SiteQuality
SIO_000300: 1.500737e6

QD
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.531862745098039e-4
allele num: 6528
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65920
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.878e1

DP
type: SiteQuality
SIO_000300: 1.500737e6

QD
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e0

VQSLOD
type: SiteQuality
SIO_000300: -3.558e0

MQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

GenotypeQuality
all individuals: 1477
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 533
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 112
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1710
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45949
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6719
bin: 6.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.518833535844471e-4
allele num: 6584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516806212838248e-5
allele num: 65928
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.617e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

QD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 5.884e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.386e0

VQSLOD
type: SiteQuality
SIO_000300: -3.844e0

DP
type: SiteQuality
SIO_000300: 1.501586e6

GenotypeQuality
all individuals: 1710
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 944
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6712
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515932450050026e-5
allele num: 65966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 8636
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.501605e6

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.111e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.84e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.415e0

FS
type: SiteQuality
SIO_000300: 3.251e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 9.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

GenotypeQuality
all individuals: 282
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 390
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 22
allele frequency: 2.194732641660016e-3
allele num: 10024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
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: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66000
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-3

QD
type: SiteQuality
SIO_000300: 1.345e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.286e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.781e0

DP
type: SiteQuality
SIO_000300: 1.497278e6

GenotypeQuality
all individuals: 349
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6431
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45380
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 910
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 3.019931548218241e-4
allele num: 9934
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.62939453125e-5
allele num: 65536
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 6.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.518e0

MQ
type: SiteQuality
SIO_000300: 5.682e1

FS
type: SiteQuality
SIO_000300: 1.8864e1

VQSLOD
type: SiteQuality
SIO_000300: -3.346e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
SIO_000300: 1.502495e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1656
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6431
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1320
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 287
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 130
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 254
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 366
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45380
bin: 6.25e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.354536950420954e-4
allele num: 6414
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.133786848072562e-3
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.373291015625e-4
allele num: 65536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9934
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: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.682e1

VQSLOD
type: SiteQuality
SIO_000300: -3.346e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
SIO_000300: 1.502495e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

FS
type: SiteQuality
SIO_000300: 1.8864e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.518e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 6.61e0

GenotypeQuality
all individuals: 397
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46394
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6763
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1736
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 11574
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: 10200
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.57e-1

FS
type: SiteQuality
SIO_000300: 3.707e0

MQRankSum
type: SiteQuality
SIO_000300: -6.32e-1

DP
type: SiteQuality
SIO_000300: 1.499583e6

QD
type: SiteQuality
SIO_000300: 1.492e1

GenotypeQuality
all individuals: 305
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1775
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6776
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66460
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: 10270
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.23e0

VQSLOD
type: SiteQuality
SIO_000300: -1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.49e-1

DP
type: SiteQuality
SIO_000300: 1.501721e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e0

QD
type: SiteQuality
SIO_000300: 1.302e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.253e0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66478
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: 11572
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.39e0

QD
type: SiteQuality
SIO_000300: 1.265e1

DP
type: SiteQuality
SIO_000300: 1.502268e6

GenotypeQuality
all individuals: 245
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1737
bin: 7.75e1
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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.699321047526673e-5
allele num: 10310
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: 8644
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.811e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.303e0

FS
type: SiteQuality
SIO_000300: 9.545999999999999e0

DP
type: SiteQuality
SIO_000300: 1.502565e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.243e1

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46821
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 1768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6798
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
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: 8644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.50683121640693e-5
allele num: 66606
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.8e0

DP
type: SiteQuality
SIO_000300: 1.505014e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.65e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 2.417e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.872e0

MQRankSum
type: SiteQuality
SIO_000300: 8.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.438e0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 418
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46801
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6801
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 9.75e1
variant carriers: 168

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 137
allele frequency: 2.055205520552055e-3
allele num: 66660
num of homozygotes: 1

South Asian
type: Population
allele count: 16
allele frequency: 9.689922480620155e-4
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.701193685021178e-4
allele num: 10388
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

FS
type: SiteQuality
SIO_000300: 5.69e-1

QD
type: SiteQuality
SIO_000300: 1.413e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.269e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

DP
type: SiteQuality
SIO_000300: 1.520224e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

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

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

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0