17-80020775-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020775
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020775
    reference: chr 17
allele count: 3
allele frequency: 2.50547027677095e-5
allele num: 119738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.472G>A
  hgvsp: ENSP00000463509.1:p.Val158Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.75G>A
  hgvsp: ENSP00000445110.2:p.Val26Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.439G>A
  hgvsp: ENSP00000463797.1:p.Val147Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.472G>A
  hgvsp: ENSP00000463962.1:p.Val158Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.472G>A
  hgvsp: ENSP00000346280.7:p.Val158Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.472G>A
  hgvsp: ENSP00000303515.5:p.Val158Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.421G>A
  hgvsp: ENSP00000463180.1:p.Val141Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.579G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.256G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val158Met
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

17-80020776-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020776
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020776
    reference: chr 17
allele count: 2
allele frequency: 1.670174032134148e-5
allele num: 119748
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.471C>T
  hgvsp: ENST00000354321.7:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.255C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.438C>T
  hgvsp: ENST00000577907.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.471C>T
  hgvsp: ENST00000306796.5:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.471C>T
  hgvsp: ENST00000582529.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.471C>T
  hgvsp: ENST00000578907.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.420C>T
  hgvsp: ENST00000578176.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.74C>T
  hgvsp: ENST00000538833.2:c.74C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.578C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41258
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr157Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

17-80020776-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020776
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020776
    reference: chr 17
allele count: 1
allele frequency: 8.350870160670742e-6
allele num: 119748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.471C>A
  hgvsp: ENST00000306796.5:c.471C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.420C>A
  hgvsp: ENST00000578176.1:c.420C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.471C>A
  hgvsp: ENST00000354321.7:c.471C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.578C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.438C>A
  hgvsp: ENST00000577907.1:c.438C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.74C>A
  hgvsp: ENST00000538833.2:c.74C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.471C>A
  hgvsp: ENST00000578907.1:c.471C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.471C>A
  hgvsp: ENST00000582529.1:c.471C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.255C>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7854
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr157Thr
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

17-80020779-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020779
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020779
    reference: chr 17
allele count: 1
allele frequency: 8.34752412434472e-6
allele num: 119796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.435G>A
  hgvsp: ENST00000577907.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.417G>A
  hgvsp: ENST00000578176.1:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.468G>A
  hgvsp: ENST00000578907.1:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.575G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.468G>A
  hgvsp: ENST00000306796.5:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.468G>A
  hgvsp: ENST00000354321.7:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.468G>A
  hgvsp: ENST00000582529.1:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.71G>A
  hgvsp: ENST00000538833.2:c.71G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.252G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2714
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys156Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

17-80020782-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020782
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020782
    reference: chr 17
allele count: 1
allele frequency: 8.346688034188035e-6
allele num: 119808
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.465C>G
  hgvsp: ENSP00000346280.7:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.465C>G
  hgvsp: ENSP00000463509.1:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.432C>G
  hgvsp: ENSP00000463797.1:p.Asp144Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.465C>G
  hgvsp: ENSP00000463962.1:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.414C>G
  hgvsp: ENSP00000463180.1:p.Asp138Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.68C>G
  hgvsp: ENSP00000445110.2:p.Asp23Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.465C>G
  hgvsp: ENSP00000303515.5:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.572C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.249C>G
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp155Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ

17-80020784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020784
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020784
    reference: chr 17
allele count: 2
allele frequency: 1.669170422300117e-5
allele num: 119820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.430G>A
  hgvsp: ENSP00000463797.1:p.Asp144Asn
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.570G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.247G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.463G>A
  hgvsp: ENSP00000303515.5:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.66G>A
  hgvsp: ENSP00000445110.2:p.Asp23Asn
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.463G>A
  hgvsp: ENSP00000463962.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.463G>A
  hgvsp: ENSP00000346280.7:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.463G>A
  hgvsp: ENSP00000463509.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.412G>A
  hgvsp: ENSP00000463180.1:p.Asp138Asn
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41281
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Asp155Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

17-80020788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020788
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020788
    reference: chr 17
allele count: 5
allele frequency: 4.172786753905728e-5
allele num: 119824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.459G>A
  hgvsp: ENST00000306796.5:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.566G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.408G>A
  hgvsp: ENST00000578176.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.62G>A
  hgvsp: ENST00000538833.2:c.62G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.243G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.459G>A
  hgvsp: ENST00000578907.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.426G>A
  hgvsp: ENST00000577907.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.459G>A
  hgvsp: ENST00000582529.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.459G>A
  hgvsp: ENST00000354321.7:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7871
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu153Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

17-80020791-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020791
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020791
    reference: chr 17
allele count: 9
allele frequency: 7.511016157030311e-5
allele num: 119824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.423G>A
  hgvsp: ENST00000577907.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.456G>A
  hgvsp: ENST00000306796.5:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.405G>A
  hgvsp: ENST00000578176.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.456G>A
  hgvsp: ENST00000578907.1:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.240G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.456G>A
  hgvsp: ENST00000354321.7:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.456G>A
  hgvsp: ENST00000582529.1:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.59G>A
  hgvsp: ENST00000538833.2:c.59G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.563G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9413
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro152Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

17-80020792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020792
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020792
    reference: chr 17
allele count: 1
allele frequency: 8.344180768332166e-6
allele num: 119844
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.455C>T
  hgvsp: ENSP00000346280.7:p.Pro152Leu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.404C>T
  hgvsp: ENSP00000463180.1:p.Pro135Leu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.455C>T
  hgvsp: ENSP00000463509.1:p.Pro152Leu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.562C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.58C>T
  hgvsp: ENSP00000445110.2:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.239C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.455C>T
  hgvsp: ENSP00000303515.5:p.Pro152Leu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.455C>T
  hgvsp: ENSP00000463962.1:p.Pro152Leu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.422C>T
  hgvsp: ENSP00000463797.1:p.Pro141Leu
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7870
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro152Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-80020801-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020801
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020801
    reference: chr 17
allele count: 2
allele frequency: 1.668474180362059e-5
allele num: 119870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.395G>A
  hgvsp: ENSP00000463180.1:p.Arg132His
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.446G>A
  hgvsp: ENSP00000463509.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.413G>A
  hgvsp: ENSP00000463797.1:p.Arg138His
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.446G>A
  hgvsp: ENSP00000303515.5:p.Arg149His
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.446G>A
  hgvsp: ENSP00000463962.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.49G>A
  hgvsp: ENSP00000445110.2:p.Arg17His
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.553G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.230G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.446G>A
  hgvsp: ENSP00000346280.7:p.Arg149His
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg149His
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-80020802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020802
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020802
    reference: chr 17
allele count: 2
allele frequency: 1.66841850609807e-5
allele num: 119874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.445C>T
  hgvsp: ENSP00000463962.1:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.445C>T
  hgvsp: ENSP00000463509.1:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.445C>T
  hgvsp: ENSP00000303515.5:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.48C>T
  hgvsp: ENSP00000445110.2:p.Arg17Cys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.229C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.412C>T
  hgvsp: ENSP00000463797.1:p.Arg138Cys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.394C>T
  hgvsp: ENSP00000463180.1:p.Arg132Cys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.445C>T
  hgvsp: ENSP00000346280.7:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.552C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41297
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg149Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum

17-80020805-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020805
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020805
    reference: chr 17
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.391A>T
  hgvsp: ENSP00000463180.1:p.Ile131Phe
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.442A>T
  hgvsp: ENSP00000303515.5:p.Ile148Phe
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.409A>T
  hgvsp: ENSP00000463797.1:p.Ile137Phe
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.442A>T
  hgvsp: ENSP00000463509.1:p.Ile148Phe
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.442A>T
  hgvsp: ENSP00000463962.1:p.Ile148Phe
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.226A>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.442A>T
  hgvsp: ENSP00000346280.7:p.Ile148Phe
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.45A>T
  hgvsp: ENSP00000445110.2:p.Ile16Phe
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.549A>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile148Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

17-80020812-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020812
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020812
    reference: chr 17
allele count: 9977
allele frequency: 8.320823325326929e-2
allele num: 119904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.384G>A
  hgvsp: ENST00000578176.1:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.219G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.435G>A
  hgvsp: ENST00000354321.7:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.435G>A
  hgvsp: ENST00000578907.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.435G>A
  hgvsp: ENST00000306796.5:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.542G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.402G>A
  hgvsp: ENST00000577907.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.38G>A
  hgvsp: ENST00000538833.2:c.38G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.435G>A
  hgvsp: ENST00000582529.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 633
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 6.75e1
  variant carriers: 766
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 536
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.25e1
  variant carriers: 402
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 8.25e1
  variant carriers: 583
genotype depth: GenotypeDepth
  all individuals: 22198
  bin: 2.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 466
genotype depth: GenotypeDepth
  all individuals: 18575
  bin: 2.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 9.75e1
  variant carriers: 1908
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 754
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 665
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.25e1
  variant carriers: 733
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 696
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 521
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.75e1
  variant carriers: 249
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 3.25e1
  variant carriers: 164
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 2
hgvs: p.Thr145Thr
num of homozygotes: 663
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS

17-80020813-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020813
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020813
    reference: chr 17
allele count: 2
allele frequency: 1.668836153666433e-5
allele num: 119844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.37C>T
  hgvsp: ENSP00000445110.2:p.Thr13Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.401C>T
  hgvsp: ENSP00000463797.1:p.Thr134Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.434C>T
  hgvsp: ENSP00000463962.1:p.Thr145Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.541C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.383C>T
  hgvsp: ENSP00000463180.1:p.Thr128Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.434C>T
  hgvsp: ENSP00000346280.7:p.Thr145Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.434C>T
  hgvsp: ENSP00000463509.1:p.Thr145Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.434C>T
  hgvsp: ENSP00000303515.5:p.Thr145Met
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.218C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr145Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/17-80020818-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020818
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020818
    reference: chr 17
allele count: 3
allele frequency: 2.504299046696829e-5
allele num: 119794
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.429T>G
  hgvsp: ENST00000354321.7:c.429T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.378T>G
  hgvsp: ENST00000578176.1:c.378T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.32T>G
  hgvsp: ENST00000538833.2:c.32T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.429T>G
  hgvsp: ENST00000578907.1:c.429T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.213T>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.396T>G
  hgvsp: ENST00000577907.1:c.396T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.429T>G
  hgvsp: ENST00000306796.5:c.429T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.429T>G
  hgvsp: ENST00000582529.1:c.429T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.536T>G
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro143Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD

17-80020820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020820
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020820
    reference: chr 17
allele count: 1
allele frequency: 8.347942232239753e-6
allele num: 119790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.427C>T
  hgvsp: ENSP00000303515.5:p.Pro143Ser
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.427C>T
  hgvsp: ENSP00000346280.7:p.Pro143Ser
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.394C>T
  hgvsp: ENSP00000463797.1:p.Pro132Ser
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.376C>T
  hgvsp: ENSP00000463180.1:p.Pro126Ser
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.211C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.427C>T
  hgvsp: ENSP00000463962.1:p.Pro143Ser
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.427C>T
  hgvsp: ENSP00000463509.1:p.Pro143Ser
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.30C>T
  hgvsp: ENSP00000445110.2:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.534C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro143Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

17-80020833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020833
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020833
    reference: chr 17
allele count: 1
allele frequency: 8.365120792344242e-6
allele num: 119544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.381G>A
  hgvsp: ENST00000577907.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.521G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.17G>A
  hgvsp: ENST00000538833.2:c.17G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.198G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.414G>A
  hgvsp: ENST00000306796.5:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.363G>A
  hgvsp: ENST00000578176.1:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.414G>A
  hgvsp: ENST00000578907.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.414G>A
  hgvsp: ENST00000582529.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.414G>A
  hgvsp: ENST00000354321.7:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu138Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD

17-80020835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020835
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020835
    reference: chr 17
allele count: 1
allele frequency: 8.370862701109976e-6
allele num: 119462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.196G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.412G>A
  hgvsp: ENSP00000463962.1:p.Glu138Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.412G>A
  hgvsp: ENSP00000303515.5:p.Glu138Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.15G>A
  hgvsp: ENSP00000445110.2:p.Glu6Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.361G>A
  hgvsp: ENSP00000463180.1:p.Glu121Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.519G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.412G>A
  hgvsp: ENSP00000346280.7:p.Glu138Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.379G>A
  hgvsp: ENSP00000463797.1:p.Glu127Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.412G>A
  hgvsp: ENSP00000463509.1:p.Glu138Lys
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44357
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu138Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

17-80020844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020844
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020844
    reference: chr 17
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.370C>T
  hgvsp: ENST00000577907.1:c.370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.187C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.403C>T
  hgvsp: ENST00000582529.1:c.403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.403C>T
  hgvsp: ENST00000306796.5:c.403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.403C>T
  hgvsp: ENST00000578907.1:c.403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.352C>T
  hgvsp: ENST00000578176.1:c.352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.510C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000445110
  ensembl transcript: ENST00000538833
  gene symbol: DUS1L
  hgvsc: ENST00000538833.2:c.6C>T
  hgvsp: ENST00000538833.2:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.403C>T
  hgvsp: ENST00000354321.7:c.403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu135Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

17-80020860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020860
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020860
    reference: chr 17
allele count: 2
allele frequency: 1.701345764499719e-5
allele num: 117554
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-11C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-11C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-11C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-11C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-11C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.494C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-11C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-11C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9248
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3077
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

17-80020868-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020868
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020868
    reference: chr 17
allele count: 1
allele frequency: 8.630659555003193e-6
allele num: 115866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-19C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-19C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-19C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-19C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.486C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-19C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-19C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-19C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1810
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5957
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

17-80020869-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020869
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020869
    reference: chr 17
allele count: 1
allele frequency: 8.6333419666753e-6
allele num: 115830
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-20G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-20G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-20G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.485G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-20G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-20G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-20G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-20G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22873
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

17-80020870-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020870
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020870
    reference: chr 17
allele count: 2
allele frequency: 1.728787774012862e-5
allele num: 115688
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-21A>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-21A>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.484A>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-21A>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-21A>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-21A>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-21A>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-21A>G
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33945
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6338
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-80020880-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020880
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020880
    reference: chr 17
allele count: 1
allele frequency: 8.765471056414571e-6
allele num: 114084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-31C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-31C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-31C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-31C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-31C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-31C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.474C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-31C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17923
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

17-80020882-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020882
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020882
    reference: chr 17
allele count: 1
allele frequency: 8.784412937683375e-6
allele num: 113838
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-33G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-33G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-33G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-33G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.472G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-33G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-33G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-33G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11151
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4990
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

17-80020888-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020888
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020888
    reference: chr 17
allele count: 3
allele frequency: 2.661131513119378e-5
allele num: 112734
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-39C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-39C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-39C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-39C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.466C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-39C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-39C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-39C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14222
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20076
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-80020894-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020894
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020894
    reference: chr 17
allele count: 1
allele frequency: 9.095539547405952e-6
allele num: 109944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-45T>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-45T>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-45T>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-45T>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-45T>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-45T>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-45T>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.460T>G
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6972
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9575
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11250
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

17-80020901-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020901
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020901
    reference: chr 17
allele count: 2
allele frequency: 1.887825413905722e-5
allele num: 105942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-52G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-52G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.453G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-52G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-52G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-52G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-52G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-52G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13567
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16118
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3761
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7951
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7489
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

17-80020902-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020902
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020902
    reference: chr 17
allele count: 27
allele frequency: 2.533213240261203e-4
allele num: 106584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-53C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-53C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-53C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-53C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-53C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-53C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.452C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-53C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16028
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13635
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11805
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 9.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 7359
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3436
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7542
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP

17-80020902-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80020902
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80020902
    reference: chr 17
allele count: 1
allele frequency: 9.382271260226676e-6
allele num: 106584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.398-53C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.398-53C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.182-53C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.398-53C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.398-53C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-53C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.452C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.365-53C>A
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11805
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16028
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7308
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3436
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7542
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

17-80021295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021295
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021295
    reference: chr 17
allele count: 1
allele frequency: 8.258729477057249e-6
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+49G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+49G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-446G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+49G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+49G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+49G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.59G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+49G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4195
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS

17-80021304-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021304
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021304
    reference: chr 17
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-455C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+40C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.50C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+40C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+40C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+40C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+40C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+40C>G
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-80021312-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021312
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021312
    reference: chr 17
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+32C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+32C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+32C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.42C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+32C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+32C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-463C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+32C>G
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4838
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

17-80021315-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021315
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021315
    reference: chr 17
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+29C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+29C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+29C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.39C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-466C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+29C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+29C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+29C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42418
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/17-80021317-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021317
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021317
    reference: chr 17
allele count: 43
allele frequency: 3.550491288910907e-4
allele num: 121110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+27G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+27G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+27G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+27G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-468G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.37G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+27G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+27G>T
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 9.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2898
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

17-80021317-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021317
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021317
    reference: chr 17
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+27G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+27G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.37G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+27G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+27G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-468G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+27G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+27G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42419
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

17-80021325-A-ATCCAGCCAACTCAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021325
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021339
    reference: chr 17
allele count: 2
allele frequency: 1.651336757104876e-5
allele num: 121114
alternate allele: ATCCAGCCAACTCAC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1455
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2319
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2488
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

17-80021330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021330
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021330
    reference: chr 17
allele count: 1
allele frequency: 8.256138438929344e-6
allele num: 121122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.24G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+14G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+14G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+14G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+14G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-481G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+14G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+14G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4974
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

17-80021333-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021333
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021333
    reference: chr 17
allele count: 1
allele frequency: 8.256411103221652e-6
allele num: 121118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-484T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+11T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+11T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+11T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.21T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+11T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+11T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+11T>C
  variant of: http://identifiers.org/hgnc/30086
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2485
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2898
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-80021341-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021341
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021341
    reference: chr 17
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.397+3G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.364+3G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.397+3G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.397+3G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.181+3G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.397+3G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578846
  gene symbol: DUS1L
  hgvsc: ENST00000578846.1:n.13G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-492G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42405
  bin: 9.75e1
  variant carriers: 1
hgvs: c.397+3G>A
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: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

17-80021364-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021364
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021364
    reference: chr 17
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.377G>A
  hgvsp: ENSP00000463962.1:p.Trp126Ter
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.377G>A
  hgvsp: ENSP00000303515.5:p.Trp126Ter
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.377G>A
  hgvsp: ENSP00000346280.7:p.Trp126Ter
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.161G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.344G>A
  hgvsp: ENSP00000463797.1:p.Trp115Ter
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.377G>A
  hgvsp: ENSP00000463509.1:p.Trp126Ter
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-515G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42404
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Trp126Ter
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-80021365-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021365
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021365
    reference: chr 17
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.376T>C
  hgvsp: ENSP00000346280.7:p.Trp126Arg
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.376T>C
  hgvsp: ENSP00000303515.5:p.Trp126Arg
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.160T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-516T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.376T>C
  hgvsp: ENSP00000463509.1:p.Trp126Arg
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.376T>C
  hgvsp: ENSP00000463962.1:p.Trp126Arg
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.343T>C
  hgvsp: ENSP00000463797.1:p.Trp115Arg
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2467
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Trp126Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

17-80021366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021366
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021366
    reference: chr 17
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.375G>A
  hgvsp: ENST00000354321.7:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.375G>A
  hgvsp: ENST00000306796.5:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-517G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.342G>A
  hgvsp: ENST00000577907.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.375G>A
  hgvsp: ENST00000578907.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.159G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.375G>A
  hgvsp: ENST00000582529.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42404
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2466
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu125Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

17-80021368-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021368
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021368
    reference: chr 17
allele count: 7
allele frequency: 5.78311660415393e-5
allele num: 121042
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.373G>A
  hgvsp: ENSP00000346280.7:p.Glu125Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.373G>A
  hgvsp: ENSP00000463509.1:p.Glu125Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.373G>A
  hgvsp: ENSP00000303515.5:p.Glu125Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.157G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.373G>A
  hgvsp: ENSP00000463962.1:p.Glu125Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.340G>A
  hgvsp: ENSP00000463797.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-519G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2467
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu125Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

17-80021369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021369
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021369
    reference: chr 17
allele count: 5
allele frequency: 4.130729321569016e-5
allele num: 121044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.372C>T
  hgvsp: ENST00000306796.5:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.372C>T
  hgvsp: ENST00000582529.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.372C>T
  hgvsp: ENST00000578907.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.339C>T
  hgvsp: ENST00000577907.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.156C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.372C>T
  hgvsp: ENST00000354321.7:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-520C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2550
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1259
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp124Asp
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-80021374-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021374
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021374
    reference: chr 17
allele count: 3
allele frequency: 2.478847170809096e-5
allele num: 121024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.367C>G
  hgvsp: ENSP00000303515.5:p.Gln123Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.334C>G
  hgvsp: ENSP00000463797.1:p.Gln112Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.367C>G
  hgvsp: ENSP00000463509.1:p.Gln123Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.367C>G
  hgvsp: ENSP00000463962.1:p.Gln123Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.367C>G
  hgvsp: ENSP00000346280.7:p.Gln123Glu
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.151C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-525C>G
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4942
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln123Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

17-80021382-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021382
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021382
    reference: chr 17
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.359C>T
  hgvsp: ENSP00000463509.1:p.Ala120Val
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.359C>T
  hgvsp: ENSP00000463962.1:p.Ala120Val
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.326C>T
  hgvsp: ENSP00000463797.1:p.Ala109Val
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.359C>T
  hgvsp: ENSP00000346280.7:p.Ala120Val
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-533C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.143C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.359C>T
  hgvsp: ENSP00000303515.5:p.Ala120Val
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42399
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2551
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala120Val
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

17-80021383-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021383
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021383
    reference: chr 17
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.358G>A
  hgvsp: ENSP00000346280.7:p.Ala120Thr
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.325G>A
  hgvsp: ENSP00000463797.1:p.Ala109Thr
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.358G>A
  hgvsp: ENSP00000463509.1:p.Ala120Thr
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-534G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.358G>A
  hgvsp: ENSP00000303515.5:p.Ala120Thr
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.358G>A
  hgvsp: ENSP00000463962.1:p.Ala120Thr
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.142G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4935
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala120Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

17-80021384-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021384
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021384
    reference: chr 17
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.324C>T
  hgvsp: ENST00000577907.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.357C>T
  hgvsp: ENST00000582529.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.357C>T
  hgvsp: ENST00000578907.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.357C>T
  hgvsp: ENST00000306796.5:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.357C>T
  hgvsp: ENST00000354321.7:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-535C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.141C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly119Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-80021399-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021399
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021399
    reference: chr 17
allele count: 6
allele frequency: 4.962450789029675e-5
allele num: 120908
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-550T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-5T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-5T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-5T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-5T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-5T>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-5T>C
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.347-5T>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD

17-80021401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021401
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021401
    reference: chr 17
allele count: 1
allele frequency: 8.272119647938589e-6
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-7C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-552C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-7C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-7C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-7C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-7C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-7C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: c.347-7C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

17-80021402-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021402
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021402
    reference: chr 17
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-8C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-8C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-553C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-8C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-8C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-8C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-8C>G
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2416
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2291
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42396
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: c.347-8C>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

17-80021408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021408
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021408
    reference: chr 17
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-14C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-14C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-559C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-14C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-14C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-14C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-14C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4596
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42396
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

17-80021413-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021413
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021413
    reference: chr 17
allele count: 8
allele frequency: 6.657124787804147e-5
allele num: 120172
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-19C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-19C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-19C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-19C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-564C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-19C>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-19C>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2512
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4465
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS

17-80021422-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021422
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021422
    reference: chr 17
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-573C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-28C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42053
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

17-80021422-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021422
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021421
    reference: chr 17
allele count: 2
allele frequency: 1.657852417977751e-5
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-29delG
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-29delG
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-29delG
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-29delG
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-574delG
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-29delG
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-29delG
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2559
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: GC
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-80021423-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021423
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021423
    reference: chr 17
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-574G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-29G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-29G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-29G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-29G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-29G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-29G>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42051
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-80021425-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021425
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021425
    reference: chr 17
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-31G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-31G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-31G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-31G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-31G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.347-576G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-31G>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2558
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

17-80021426-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021426
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021424
    reference: chr 17
allele count: 1
allele frequency: 8.29132395860971e-6
allele num: 120608
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-34_347-33delCA
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+574_346+575delCA
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-34_347-33delCA
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-34_131-33delCA
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-34_347-33delCA
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-34_347-33delCA
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-34_314-33delCA
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42052
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: CTG
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

17-80021440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021440
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021440
    reference: chr 17
allele count: 15
allele frequency: 1.245288657910904e-4
allele num: 120454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-46C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+562C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-46C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-46C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-46C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-46C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-46C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

17-80021442-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021442
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021442
    reference: chr 17
allele count: 1
allele frequency: 8.304268393954492e-6
allele num: 120420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-48C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-48C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-48C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+560C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-48C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-48C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-48C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2920
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

17-80021442-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021442
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021442
    reference: chr 17
allele count: 1
allele frequency: 8.304268393954492e-6
allele num: 120420
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-48C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-48C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-48C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-48C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-48C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-48C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+560C>G
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

17-80021445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021445
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021445
    reference: chr 17
allele count: 1
allele frequency: 8.309788931361144e-6
allele num: 120340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.347-51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.314-51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.131-51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.347-51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+557C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.347-51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.347-51C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6017
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2920
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-80021951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021951
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021951
    reference: chr 17
allele count: 7
allele frequency: 8.095854922279793e-5
allele num: 86464
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.346+51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.346+51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.346+51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.130+51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.346+51C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.313+51C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12053
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13904
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19811
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8661
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

17-80021951-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021951
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021951
    reference: chr 17
allele count: 2
allele frequency: 2.313101406365655e-5
allele num: 86464
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.346+51C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.346+51C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.346+51C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.130+51C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.346+51C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+51C>G
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.313+51C>G
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12053
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19811
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5338
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8661
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-80021961-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021961
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021961
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 86820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.130+41C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.346+41C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.313+41C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.346+41C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.346+41C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+41C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.346+41C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13856
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3011
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13096
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

17-80021963-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021963
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021963
    reference: chr 17
allele count: 5
allele frequency: 5.706720233747261e-5
allele num: 87616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.130+39G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.346+39G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.346+39G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+39G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.346+39G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.346+39G>A
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.313+39G>A
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5316
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8423
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6413
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2607
  bin: 4.75e1
  variant carriers: 0
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: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD

17-80021971-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021971
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021971
    reference: chr 17
allele count: 7
allele frequency: 7.798052714836352e-5
allele num: 89766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.313+31G>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.346+31G>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.346+31G>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+31G>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.130+31G>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.346+31G>C
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.346+31G>C
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14791
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13548
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7540
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4934
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

17-80021974-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021974
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021974
    reference: chr 17
allele count: 1
allele frequency: 1.099868015838099e-5
allele num: 90920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.130+28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.346+28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.346+28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.346+28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.346+28C>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.313+28C>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6820
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-80021977-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021977
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021977
    reference: chr 17
allele count: 40
allele frequency: 4.347259053166978e-4
allele num: 92012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+25G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.346+25G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.346+25G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.130+25G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.346+25G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.313+25G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.346+25G>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13637
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12771
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20210
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2213
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4328
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3564
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13549
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-80021987-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80021987
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80021987
    reference: chr 17
allele count: 2
allele frequency: 2.023513223658917e-5
allele num: 98838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl transcript: ENST00000578264
  gene symbol: DUS1L
  hgvsc: ENST00000578264.1:n.130+15G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000303515
  ensembl transcript: ENST00000306796
  gene symbol: DUS1L
  hgvsc: ENST00000306796.5:c.346+15G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000346280
  ensembl transcript: ENST00000354321
  gene symbol: DUS1L
  hgvsc: ENST00000354321.7:c.346+15G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463509
  ensembl transcript: ENST00000582529
  gene symbol: DUS1L
  hgvsc: ENST00000582529.1:c.346+15G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463962
  ensembl transcript: ENST00000578907
  gene symbol: DUS1L
  hgvsc: ENST00000578907.1:c.346+15G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463180
  ensembl transcript: ENST00000578176
  gene symbol: DUS1L
  hgvsc: ENST00000578176.1:c.346+15G>T
  variant of: http://identifiers.org/hgnc/30086
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169718
  ensembl protein: ENSP00000463797
  ensembl transcript: ENST00000577907
  gene symbol: DUS1L
  hgvsc: ENST00000577907.1:c.313+15G>T
  variant of: http://identifiers.org/hgnc/30086
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8042
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10962
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2473
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41251
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1733
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7852
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 883
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.057355998532469e-5
allele num: 65416
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

FS
type: SiteQuality
SIO_000300: 2.291e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

QD
type: SiteQuality
SIO_000300: 1.183e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.605442e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.514692517418964e-4
allele num: 6602
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.736e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.606123e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

QD
type: SiteQuality
SIO_000300: 1.152e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.800078400627205e-5
allele num: 10204
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65422
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.606123e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

FS
type: SiteQuality
SIO_000300: 1.736e0

QD
type: SiteQuality
SIO_000300: 1.152e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.790483649892304e-5
allele num: 10214
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65462
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.119e-1

FS
type: SiteQuality
SIO_000300: 8.667999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

DP
type: SiteQuality
SIO_000300: 1.606377e6

QD
type: SiteQuality
SIO_000300: 1.025e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.287e0

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.207e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.143e1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.38e-1

DP
type: SiteQuality
SIO_000300: 1.606678e6

FS
type: SiteQuality
SIO_000300: 8.29e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.054367745876604e-5
allele num: 65480
num of homozygotes: 0

South Asian
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num of homozygotes: 0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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QD
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.636385851304295e-5
allele num: 65476
num of homozygotes: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6602
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South Asian
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DP
type: SiteQuality
SIO_000300: 1.607402e6

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.221859058557595e-4
allele num: 65474
num of homozygotes: 0

South Asian
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African
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Other
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East Asian
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allele count: 0
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European (Finnish)
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DP
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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QD
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BaseQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.942e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52699731248473e-5
allele num: 65488
num of homozygotes: 0

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

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

European (Finnish)
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East Asian
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South Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.429e0

VQSLOD
type: SiteQuality
SIO_000300: -8.672e-1

QD
type: SiteQuality
SIO_000300: 2.971e1

MQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

DP
type: SiteQuality
SIO_000300: 1.607889e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2705
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526857422053929e-5
allele num: 65494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

QD
type: SiteQuality
SIO_000300: 3.02e1

MQRankSum
type: SiteQuality
SIO_000300: -3.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.608124e6

FS
type: SiteQuality
SIO_000300: 4.501e0

VQSLOD
type: SiteQuality
SIO_000300: -2.943e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
all individuals: 2705
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053621595211921e-5
allele num: 65496
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.93e1

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.92e-1

DP
type: SiteQuality
SIO_000300: 1.608376e6

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.337e1

FS
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.23e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 883
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variant carriers: 0

GenotypeQuality
all individuals: 7869
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
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: 10236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

QD
type: SiteQuality
SIO_000300: 8.5e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

DP
type: SiteQuality
SIO_000300: 1.608218e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.321e0

MQRankSum
type: SiteQuality
SIO_000300: -1.368e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 8.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.602e0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 391
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variant carriers: 9

GenotypeQuality
all individuals: 38037
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 32
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variant carriers: 9

GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 9998
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variant carriers: 9247

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 2376
allele frequency: 2.317596566523605e-1
allele num: 10252
num of homozygotes: 299

Other
type: Population
allele count: 76
allele frequency: 8.53932584269663e-2
allele num: 890
num of homozygotes: 6

East Asian
type: Population
allele count: 397
allele frequency: 4.616279069767442e-2
allele num: 8600
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 3375
allele frequency: 5.151098901098901e-2
allele num: 65520
num of homozygotes: 91

South Asian
type: Population
allele count: 1776
allele frequency: 1.076363636363636e-1
allele num: 16500
num of homozygotes: 124

Latino
type: Population
allele count: 1594
allele frequency: 1.381043146768324e-1
allele num: 11542
num of homozygotes: 121

European (Finnish)
type: Population
allele count: 383
allele frequency: 5.803030303030303e-2
allele num: 6600
num of homozygotes: 16

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.31e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.276e1

DP
type: SiteQuality
SIO_000300: 2.039222e6

FS
type: SiteQuality
SIO_000300: 1.161e0

GenotypeQuality
all individuals: 2025
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 907
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variant carriers: 2

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 1090
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 44893
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 431
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GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65486
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.44e-1

FS
type: SiteQuality
SIO_000300: 4.056e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: -1.652e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 1.603416e6

QD
type: SiteQuality
SIO_000300: 1.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2001
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GenotypeQuality
all individuals: 905
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 3
allele frequency: 2.935995302407516e-4
allele num: 10218
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65460
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.993e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 1.601709e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

FS
type: SiteQuality
SIO_000300: 1.8882e1

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-1

QD
type: SiteQuality
SIO_000300: 8.42e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1084
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
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: 8596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527603800678256e-5
allele num: 65462
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.077e0

FS
type: SiteQuality
SIO_000300: 1.401e0

DP
type: SiteQuality
SIO_000300: 1.601657e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 6.91e0

VQSLOD
type: SiteQuality
SIO_000300: -7.61e-2

GenotypeQuality
all individuals: 301
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 366
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 2012
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GenotypeQuality
all individuals: 770
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GenotypeQuality
all individuals: 429
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1989
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GenotypeQuality
all individuals: 900
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variant carriers: 1

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65330
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.832841691248771e-5
allele num: 10170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.596891e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

FS
type: SiteQuality
SIO_000300: 3.388e0

QD
type: SiteQuality
SIO_000300: 1.185e1

GenotypeQuality
all individuals: 2002
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 306
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1981
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7806
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
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: 16484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531862745098039e-5
allele num: 65280
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 2.226e0

DP
type: SiteQuality
SIO_000300: 1.595429e6

MQRankSum
type: SiteQuality
SIO_000300: -5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.378e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

QD
type: SiteQuality
SIO_000300: 2.22e1

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7683
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variant carriers: 0

GenotypeQuality
all individuals: 865
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variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1938
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variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
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variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537468097536976e-5
allele num: 65042
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.397e1

DP
type: SiteQuality
SIO_000300: 1.585768e6

MQRankSum
type: SiteQuality
SIO_000300: 5.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.266e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
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variant carriers: 0

GenotypeQuality
all individuals: 390
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variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40837
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 7.25e1
variant carriers: 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: 872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64202
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.764290755116443e-4
allele num: 11336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.177e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.188e0

FS
type: SiteQuality
SIO_000300: 1.588e0

QD
type: SiteQuality
SIO_000300: 1.055e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-1

DP
type: SiteQuality
SIO_000300: 1.536843e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 986
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variant carriers: 0

GenotypeQuality
all individuals: 533
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1737
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6433
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variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63254
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.211240310077519e-4
allele num: 8256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

DP
type: SiteQuality
SIO_000300: 1.453622e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.635e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.113e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.228e1

GenotypeQuality
all individuals: 329
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34817
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5982
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variant carriers: 0

GenotypeQuality
all individuals: 1797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
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variant carriers: 0

GenotypeQuality
all individuals: 6388
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variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.581177661122004e-5
allele num: 63244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 9.59e0

VQSLOD
type: SiteQuality
SIO_000300: -5.695e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 1.452867e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.458e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.117e0

GenotypeQuality
all individuals: 493
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
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variant carriers: 0

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 570
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variant carriers: 0

GenotypeQuality
all individuals: 6370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 2266
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variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
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variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.166160081053698e-5
allele num: 63168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11136
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

DP
type: SiteQuality
SIO_000300: 1.439574e6

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.23e-1

FS
type: SiteQuality
SIO_000300: 8.804e0

QD
type: SiteQuality
SIO_000300: 1.635e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
all individuals: 684
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 334
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variant carriers: 0

GenotypeQuality
all individuals: 155
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variant carriers: 0

GenotypeQuality
all individuals: 464
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GenotypeQuality
all individuals: 3262
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4464
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variant carriers: 0

GenotypeQuality
all individuals: 5285
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.590330788804071e-4
allele num: 6288
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8056
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10980
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.748e0

QD
type: SiteQuality
SIO_000300: 1.646e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.2e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

MQ
type: SiteQuality
SIO_000300: 5.813e1

DP
type: SiteQuality
SIO_000300: 1.32706e6

GenotypeQuality
all individuals: 9669
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 7.5e0
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GenotypeQuality
all individuals: 667
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variant carriers: 0

GenotypeQuality
all individuals: 3291
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3572
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
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variant carriers: 0

GenotypeQuality
all individuals: 24034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
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variant carriers: 0

GenotypeQuality
all individuals: 985
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variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10958
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.244090569793481e-4
allele num: 8038
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16040
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.447e0

MQRankSum
type: SiteQuality
SIO_000300: -6.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.244e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.41e0

VQSLOD
type: SiteQuality
SIO_000300: -1.839e0

DP
type: SiteQuality
SIO_000300: 1.301655e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

GenotypeQuality
all individuals: 975
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10193
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 319
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GenotypeQuality
all individuals: 6196
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9428
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10850
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.880877742946708e-4
allele num: 15950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.927e0

QD
type: SiteQuality
SIO_000300: 1.168e1

DP
type: SiteQuality
SIO_000300: 1.247299e6

MQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.412650602409639e-5
allele num: 10624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8916
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.046e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.06e-1

QD
type: SiteQuality
SIO_000300: 7.99e0

MQRankSum
type: SiteQuality
SIO_000300: 3.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e0

DP
type: SiteQuality
SIO_000300: 1.16585e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1125
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GenotypeQuality
all individuals: 2752
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5930
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.441748408191361e-5
allele num: 58110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7998
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7328
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

DP
type: SiteQuality
SIO_000300: 1.130259e6

FS
type: SiteQuality
SIO_000300: 6.133e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

VQSLOD
type: SiteQuality
SIO_000300: -3.667e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 2.342786683107275e-3
allele num: 8110
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.208007185936096e-4
allele num: 15586
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.703085581214826e-5
allele num: 10306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.424422984727073e-5
allele num: 58404
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

FS
type: SiteQuality
SIO_000300: 1.421e0

DP
type: SiteQuality
SIO_000300: 1.128835e6

GenotypeQuality
all individuals: 5481
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
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variant carriers: 1

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

GenotypeQuality
all individuals: 1144
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variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.712211492363537e-5
allele num: 58404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.421e0

DP
type: SiteQuality
SIO_000300: 1.128835e6

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

QD
type: SiteQuality
SIO_000300: 1.38e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

GenotypeQuality
all individuals: 2326
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 132
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 2419
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: -3.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.162e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.465561e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 50
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2435
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GenotypeQuality
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GenotypeQuality
all individuals: 42418
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 10376
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 66488
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

DP
type: SiteQuality
SIO_000300: 3.467832e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 2.545e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: -2.3e0

QD
type: SiteQuality
SIO_000300: 1.047e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.375e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 180
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.428e0

DP
type: SiteQuality
SIO_000300: 3.469608e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-2

QD
type: SiteQuality
SIO_000300: 1.186e1

VQSLOD
type: SiteQuality
SIO_000300: -7.658e-1

FS
type: SiteQuality
SIO_000300: 5.132e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.421e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 30
bin: 4.75e1
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GenotypeQuality
all individuals: 2897
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GenotypeQuality
all individuals: 2553
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
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: 10376
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.469612e6

MQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-2

FS
type: SiteQuality
SIO_000300: 1.749e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.226e0

QD
type: SiteQuality
SIO_000300: 1.262e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.657e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 43

GenotypeQuality
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GenotypeQuality
all individuals: 2471
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 1262
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 39
allele frequency: 3.759398496240601e-3
allele num: 10374
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: 906
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.457216940363008e-4
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.04e-1

DP
type: SiteQuality
SIO_000300: 3.471789e6

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.732e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.145e1

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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African
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Other
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Latino
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European (Non-Finnish)
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FS
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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Other
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South Asian
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European (Finnish)
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African
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DP
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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DP
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Latino
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African
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East Asian
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Other
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European (Finnish)
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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DP
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ClippingRankSum
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QD
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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allele num: 66450
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Latino
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European (Finnish)
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South Asian
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Other
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MQ
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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Latino
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African
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Other
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European (Non-Finnish)
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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Other
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Latino
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African
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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FS
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.010144185906505e-5
allele num: 66442
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
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MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.431e0

MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.16e-1

FS
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QD
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
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: 66422
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.183e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

FS
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SIO_000300: 3.623e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e-1

VQSLOD
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

DP
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SIO_000300: 3.462316e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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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: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506069459923492e-5
allele num: 66398
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.62e-1

FS
type: SiteQuality
SIO_000300: 4.027e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.716e0

MQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

DP
type: SiteQuality
SIO_000300: 3.461197e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506114826194349e-5
allele num: 66396
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 7.86e-1

QD
type: SiteQuality
SIO_000300: 9.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.259e0

VQSLOD
type: SiteQuality
SIO_000300: -1.868e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

DP
type: SiteQuality
SIO_000300: 3.461061e6

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 49
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 904
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: 1
allele frequency: 1.506341698550899e-5
allele num: 66386
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.460905e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.277e1

FS
type: SiteQuality
SIO_000300: 1.852e0

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

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

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507704369327262e-5
allele num: 66326
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.42306760358614e-4
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.458369e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 2.142e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

QD
type: SiteQuality
SIO_000300: 1.275e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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South Asian
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allele frequency: 0.0e0
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East Asian
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQRankSum
type: SiteQuality
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QD
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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FS
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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allele num: 11564
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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East Asian
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allele num: 8636
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South Asian
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allele count: 1
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allele num: 16508
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66296
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InbreedingCoeff
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MQ
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele count: 1
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allele num: 66254
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Other
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VQSLOD
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ReadPosRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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QD
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 2
allele frequency: 1.947040498442368e-4
allele num: 10272
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.585411736149038e-5
allele num: 65916
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 6538
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East Asian
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allele num: 8528
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South Asian
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Other
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BaseQRankSum
type: SiteQuality
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VQSLOD
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DP
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MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.8e-1

FS
type: SiteQuality
SIO_000300: 1.324e1

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

GenotypeQuality
all individuals: 4605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2923
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 11562
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.742e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 1.702e1

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 5.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

DP
type: SiteQuality
SIO_000300: 3.425438e6

GenotypeQuality
all individuals: 2923
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42053
bin: 9.75e1
variant carriers: 2

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: 8636
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.937608990505716e-4
allele num: 10322
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: 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: 66106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.425438e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.702e1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.742e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 5.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

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

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2398
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2557
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2922
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66094
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.576e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.243e0

DP
type: SiteQuality
SIO_000300: 3.424996e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.52e-1

QD
type: SiteQuality
SIO_000300: 1.538e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.522e0

GenotypeQuality
all individuals: 4556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42052
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 140
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1467
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
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: 902
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: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.946e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.15e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.308e0

DP
type: SiteQuality
SIO_000300: 3.424196e6

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

GenotypeQuality
all individuals: 498
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2558
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2922
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4506
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513179796023364e-5
allele num: 66086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.808e1

DP
type: SiteQuality
SIO_000300: 3.423605e6

GenotypeQuality
all individuals: 468
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42044
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2923
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
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: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.111239860950173e-4
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.718172983479106e-5
allele num: 10290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.061088373503107e-4
allele num: 65970
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.986e0

DP
type: SiteQuality
SIO_000300: 3.412614e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

QD
type: SiteQuality
SIO_000300: 1.354e1

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

GenotypeQuality
all individuals: 428
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2259
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42042
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2538
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65958
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-1

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.008e0

DP
type: SiteQuality
SIO_000300: 3.410433e6

GenotypeQuality
all individuals: 2538
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42042
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 417
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
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: 8626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.008e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-2

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
type: SiteQuality
SIO_000300: 3.410433e6

GenotypeQuality
all individuals: 397
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42040
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2061
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2526
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51758885482745e-5
allele num: 65894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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: 11558
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.408524e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.306e1

MQRankSum
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.122e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.209e0

GenotypeQuality
all individuals: 1620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5118
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 425
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 193
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5338
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4155
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6823
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 662
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.507970702283498e-4
allele num: 46420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13640
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

DP
type: SiteQuality
SIO_000300: 8.74271e5

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.973e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 1.356e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1619
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2919
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6823
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5118
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2932
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4155
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46420
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.466275659824047e-4
allele num: 13640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.74271e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.973e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

GenotypeQuality
all individuals: 9705
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6583
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2619
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3986
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.01094e5

VQSLOD
type: SiteQuality
SIO_000300: 4.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

QD
type: SiteQuality
SIO_000300: 1.564e1

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11073
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 951
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13474
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47124
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.643252696006995e-4
allele num: 13724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7226
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 1.854e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.13786e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

QD
type: SiteQuality
SIO_000300: 1.341e1

GenotypeQuality
all individuals: 16393
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5168
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1625
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 6
allele frequency: 8.138903960933261e-4
allele num: 7372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.187084520417854e-4
allele num: 8424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4218
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.076e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.538e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

QD
type: SiteQuality
SIO_000300: 8.970000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.17e-1

DP
type: SiteQuality
SIO_000300: 9.72821e5

GenotypeQuality
all individuals: 4331
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4688
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19462
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.039318052043397e-5
allele num: 49036
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13986
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.002301e6

VQSLOD
type: SiteQuality
SIO_000300: -6.736e-1

FS
type: SiteQuality
SIO_000300: 9.448e0

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

QD
type: SiteQuality
SIO_000300: 1.526e1

MQ
type: SiteQuality
SIO_000300: 5.91e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.28e-1

GenotypeQuality
all individuals: 746
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6023
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 934
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 9.75e1
variant carriers: 41

GenotypeQuality
all individuals: 999
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21541
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 4.610419548178884e-4
allele num: 8676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7006
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.488095238095238e-3
allele num: 672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14014
num of homozygotes: 0

African
type: Population
allele count: 35
allele frequency: 4.61133069828722e-3
allele num: 7590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49690
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.683e0

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

FS
type: SiteQuality
SIO_000300: 7.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

DP
type: SiteQuality
SIO_000300: 1.039163e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3