10-35327961-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35327961
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35327961
    reference: chr 10
allele count: 1
allele frequency: 9.290399301361972e-6
allele num: 107638
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.821A>C
  hgvsp: ENSP00000444856.1:p.His274Pro
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.764A>C
  hgvsp: ENSP00000363878.1:p.His255Pro
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.593A>C
  hgvsp: ENSP00000473659.1:p.His198Pro
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.764A>C
  hgvsp: ENSP00000363881.3:p.His255Pro
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.764A>C
  hgvsp: ENSP00000363880.1:p.His255Pro
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.764A>C
  hgvsp: ENSP00000363883.3:p.His255Pro
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*447A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.764A>C
  hgvsp: ENSP00000363874.1:p.His255Pro
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His274Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

10-35327963-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35327963
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35327963
    reference: chr 10
allele count: 1
allele frequency: 9.288328286674964e-6
allele num: 107662
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.591A>G
  hgvsp: ENST00000602371.1:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*445A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.762A>G
  hgvsp: ENST00000374748.1:c.762A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.819A>G
  hgvsp: ENST00000537177.1:c.819A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.762A>G
  hgvsp: ENST00000374742.1:c.762A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.762A>G
  hgvsp: ENST00000374751.3:c.762A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.762A>G
  hgvsp: ENST00000374746.1:c.762A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.762A>G
  hgvsp: ENST00000374749.3:c.762A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35729
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu273Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

10-35327973-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35327973
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35327973
    reference: chr 10
allele count: 1
allele frequency: 9.364874229739094e-6
allele num: 106782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*435G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.752G>A
  hgvsp: ENSP00000363883.3:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.752G>A
  hgvsp: ENSP00000363878.1:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.752G>A
  hgvsp: ENSP00000363881.3:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.581G>A
  hgvsp: ENSP00000473659.1:p.Arg194Gln
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.752G>A
  hgvsp: ENSP00000363880.1:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.752G>A
  hgvsp: ENSP00000363874.1:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.809G>A
  hgvsp: ENSP00000444856.1:p.Arg270Gln
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10190
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg270Gln
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

10-35327982-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35327982
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35327982
    reference: chr 10
allele count: 2
allele frequency: 1.89465706707086e-5
allele num: 105560
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.572T>C
  hgvsp: ENSP00000473659.1:p.Ile191Thr
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.743T>C
  hgvsp: ENSP00000363878.1:p.Ile248Thr
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.743T>C
  hgvsp: ENSP00000363874.1:p.Ile248Thr
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.743T>C
  hgvsp: ENSP00000363880.1:p.Ile248Thr
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.743T>C
  hgvsp: ENSP00000363881.3:p.Ile248Thr
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.800T>C
  hgvsp: ENSP00000444856.1:p.Ile267Thr
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*426T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.743T>C
  hgvsp: ENSP00000363883.3:p.Ile248Thr
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39961
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile267Thr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

10-35327998-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35327998
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35327998
    reference: chr 10
allele count: 1
allele frequency: 9.890022944853232e-6
allele num: 101112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.727T>C
  hgvsp: ENST00000374749.3:c.727T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*410T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.727T>C
  hgvsp: ENST00000374746.1:c.727T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.784T>C
  hgvsp: ENST00000537177.1:c.784T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.727T>C
  hgvsp: ENST00000374751.3:c.727T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.727T>C
  hgvsp: ENST00000374742.1:c.727T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.727T>C
  hgvsp: ENST00000374748.1:c.727T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.556T>C
  hgvsp: ENST00000602371.1:c.556T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27970
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2849
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu262Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

10-35328002-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328002
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328002
    reference: chr 10
allele count: 2
allele frequency: 2.016494928515255e-5
allele num: 99182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*406T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.723T>A
  hgvsp: ENST00000374749.3:c.723T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.723T>A
  hgvsp: ENST00000374751.3:c.723T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.780T>A
  hgvsp: ENST00000537177.1:c.780T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.723T>A
  hgvsp: ENST00000374746.1:c.723T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.723T>A
  hgvsp: ENST00000374748.1:c.723T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.723T>A
  hgvsp: ENST00000374742.1:c.723T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.552T>A
  hgvsp: ENST00000602371.1:c.552T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25653
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8706
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2848
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly260Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

10-35328013-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328013
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328013
    reference: chr 10
allele count: 1
allele frequency: 1.0395874916833e-5
allele num: 96192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-3T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-3T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-3T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-3T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-3T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-3T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-3T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-3T>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
hgvs: c.772-3T>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

10-35328025-T-TAAATAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328025
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328031
    reference: chr 10
allele count: 1
allele frequency: 1.088115601401493e-5
allele num: 91902
alternate allele: TAAATAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-16_715-15insTTATTT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-16_715-15insTTATTT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-16_715-15insTTATTT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-16_*398-15insTTATTT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-16_772-15insTTATTT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-16_544-15insTTATTT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-16_715-15insTTATTT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-16_715-15insTTATTT
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16097
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3617
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19824
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

10-35328026-C-CCTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328026
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328029
    reference: chr 10
allele count: 1
allele frequency: 1.09644313845884e-5
allele num: 91204
alternate allele: CCTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-17_715-16insAAG
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-17_715-16insAAG
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-17_544-16insAAG
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-17_*398-16insAAG
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-17_772-16insAAG
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-17_715-16insAAG
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-17_715-16insAAG
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-17_715-16insAAG
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16404
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19818
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2410
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-35328046-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328046
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328046
    reference: chr 10
allele count: 2
allele frequency: 2.383960712327461e-5
allele num: 83894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-36C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-36C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-36C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-36C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-36C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-36C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-36C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-36C>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17246
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7914
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

10-35328048-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328048
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328048
    reference: chr 10
allele count: 1
allele frequency: 1.194143918225025e-5
allele num: 83742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-38A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-38A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-38A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-38A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-38A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-38A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-38A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-38A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9924
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4763
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4632
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7844
  bin: 6.25e1
  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: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

10-35328050-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328050
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328050
    reference: chr 10
allele count: 1
allele frequency: 1.207437816952427e-5
allele num: 82820
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-40A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-40A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-40A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-40A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-40A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-40A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-40A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-40A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6844
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4775
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2657
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

10-35328052-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328052
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328051
    reference: chr 10
allele count: 1
allele frequency: 1.227174553308463e-5
allele num: 81488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-43delA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-43delA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-43delA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-43delA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-43delA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-43delA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-43delA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-43delA
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17058
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4724
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4841
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6804
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: CT
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

10-35328056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328056
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328056
    reference: chr 10
allele count: 1
allele frequency: 1.249063202598051e-5
allele num: 80060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-46C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-46C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-46C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-46C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-46C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-46C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-46C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-46C>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16453
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6824
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4701
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3188
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14746
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-35328058-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35328058
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35328058
    reference: chr 10
allele count: 1
allele frequency: 1.269389931199066e-5
allele num: 78778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.715-48C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.715-48C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.544-48C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*398-48C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.772-48C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.715-48C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.715-48C>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.715-48C>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10513
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4676
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3077
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3329
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4805
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/10-35333445-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333445
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333445
    reference: chr 10
allele count: 5
allele frequency: 5.053567818880129e-5
allele num: 98940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+49T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+49T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+49T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+49T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+49T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+49T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+49T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+49T>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16836
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12588
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9369
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1922
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5031
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7551
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8935
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-35333446-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333446
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333446
    reference: chr 10
allele count: 1
allele frequency: 1.010386776057875e-5
allele num: 98972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+48C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+48C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+48C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+48C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+48C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+48C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+48C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+48C>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3287
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4983
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7097
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

10-35333451-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333451
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333451
    reference: chr 10
allele count: 2
allele frequency: 2.015763268761716e-5
allele num: 99218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+43C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+43C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+43C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+43C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+43C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+43C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+43C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+43C>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12699
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16440
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6452
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/10-35333452-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333452
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333452
    reference: chr 10
allele count: 2
allele frequency: 2.004249007896741e-5
allele num: 99788
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+42T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+42T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+42T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+42T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+42T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+42T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+42T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+42T>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16299
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8760
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6883
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6376
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3287
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

10-35333452-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333452
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333452
    reference: chr 10
allele count: 1
allele frequency: 1.002124503948371e-5
allele num: 99788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+42T>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3287
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6883
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6376
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2784
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4056
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

10-35333460-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333460
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333460
    reference: chr 10
allele count: 1
allele frequency: 9.910999226942061e-6
allele num: 100898
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+34A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6044
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9177
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

10-35333464-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333464
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333464
    reference: chr 10
allele count: 1
allele frequency: 9.863878477017164e-6
allele num: 101380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+30A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+30A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+30A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+30A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+30A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+30A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+30A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+30A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9066
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22703
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3751
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9052
  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: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

10-35333468-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333468
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333468
    reference: chr 10
allele count: 2
allele frequency: 1.946282600233554e-5
allele num: 102760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+26A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+26A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+26A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+26A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+26A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+26A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+26A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+26A>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6985
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8656
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2959
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2869
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

10-35333471-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333471
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333471
    reference: chr 10
allele count: 1
allele frequency: 9.572675754326849e-6
allele num: 104464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+23T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+23T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+23T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+23T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+23T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+23T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+23T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+23T>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28308
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29755
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

10-35333474-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333474
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333474
    reference: chr 10
allele count: 1
allele frequency: 9.427914168269412e-6
allele num: 106068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+20G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+20G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+20G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+20G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+20G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+20G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+20G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+20G>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32295
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7254
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

10-35333475-GAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333475
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333473
    reference: chr 10
allele count: 1
allele frequency: 9.327662114767555e-6
allele num: 107208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+17_714+18delAT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+17_714+18delAT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+17_714+18delAT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+17_543+18delAT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+17_714+18delAT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+17_771+18delAT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+17_714+18delAT
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+17_*397+18delAT
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: GAT
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

10-35333476-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333476
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333476
    reference: chr 10
allele count: 1
allele frequency: 9.230201218386561e-6
allele num: 108340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+18T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+18T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+18T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+18T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+18T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+18T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+18T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+18T>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8657
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 5.25e1
  variant carriers: 0
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: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

10-35333477-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333477
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333477
    reference: chr 10
allele count: 3
allele frequency: 2.75471975317711e-5
allele num: 108904
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+17A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+17A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+17A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+17A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+17A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+17A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+17A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+17A>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8749
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33161
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

10-35333478-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333478
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333478
    reference: chr 10
allele count: 1
allele frequency: 9.115604091083115e-6
allele num: 109702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+16T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+16T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+16T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+16T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+16T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+16T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+16T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+16T>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8847
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum

10-35333480-G-GTTTTATTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333480
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333488
    reference: chr 10
allele count: 1
allele frequency: 9.02233931213685e-6
allele num: 110836
alternate allele: GTTTTATTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1535
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3294
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4441
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

10-35333482-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333482
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333482
    reference: chr 10
allele count: 1
allele frequency: 8.922039221284417e-6
allele num: 112082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+12A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+12A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+12A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+12A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+12A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+12A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+12A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+12A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39162
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3298
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-35333489-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333489
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333489
    reference: chr 10
allele count: 1
allele frequency: 8.69837514352319e-6
allele num: 114964
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.771+5G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.714+5G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.543+5G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.714+5G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.714+5G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.714+5G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.714+5G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*397+5G>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4767
  bin: 6.75e1
  variant carriers: 0
hgvs: c.771+5G>T
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-35333517-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333517
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333517
    reference: chr 10
allele count: 1
allele frequency: 8.350033400133601e-6
allele num: 119760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.691A>G
  hgvsp: ENSP00000363874.1:p.Asn231Asp
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*374A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.520A>G
  hgvsp: ENSP00000473659.1:p.Asn174Asp
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.691A>G
  hgvsp: ENSP00000363883.3:p.Asn231Asp
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.691A>G
  hgvsp: ENSP00000363880.1:p.Asn231Asp
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.748A>G
  hgvsp: ENSP00000444856.1:p.Asn250Asp
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.691A>G
  hgvsp: ENSP00000363878.1:p.Asn231Asp
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.691A>G
  hgvsp: ENSP00000363881.3:p.Asn231Asp
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45663
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn250Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

10-35333540-GCTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333540
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333537
    reference: chr 10
allele count: 3
allele frequency: 2.493019545273235e-5
allele num: 120336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.665_667delAAG
  hgvsp: ENSP00000363883.3:p.Glu222del
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.665_667delAAG
  hgvsp: ENSP00000363878.1:p.Glu222del
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.722_724delAAG
  hgvsp: ENSP00000444856.1:p.Glu241del
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.665_667delAAG
  hgvsp: ENSP00000363874.1:p.Glu222del
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*348_*350delAAG
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.665_667delAAG
  hgvsp: ENSP00000363881.3:p.Glu222del
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.665_667delAAG
  hgvsp: ENSP00000363880.1:p.Glu222del
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.494_496delAAG
  hgvsp: ENSP00000473659.1:p.Glu165del
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3302
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5306
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu241del
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: GCTT
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

10-35333559-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333559
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333559
    reference: chr 10
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.706G>A
  hgvsp: ENSP00000444856.1:p.Glu236Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.478G>A
  hgvsp: ENSP00000473659.1:p.Glu160Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.649G>A
  hgvsp: ENST00000421317.1:c.649G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.649G>A
  hgvsp: ENSP00000363880.1:p.Glu217Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.649G>A
  hgvsp: ENSP00000363874.1:p.Glu217Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*332G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.649G>A
  hgvsp: ENSP00000363881.3:p.Glu217Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.649G>A
  hgvsp: ENSP00000363878.1:p.Glu217Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.649G>A
  hgvsp: ENSP00000363883.3:p.Glu217Lys
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu236Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

10-35333563-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333563
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333563
    reference: chr 10
allele count: 1
allele frequency: 8.307165761185599e-6
allele num: 120378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.645A>T
  hgvsp: ENST00000421317.1:c.645A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*328A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.474A>T
  hgvsp: ENST00000602371.1:c.474A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.645A>T
  hgvsp: ENST00000374746.1:c.645A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.645A>T
  hgvsp: ENST00000374749.3:c.645A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.645A>T
  hgvsp: ENST00000374751.3:c.645A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.645A>T
  hgvsp: ENST00000374748.1:c.645A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.702A>T
  hgvsp: ENST00000537177.1:c.702A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.645A>T
  hgvsp: ENST00000374742.1:c.645A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5301
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr234Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

10-35333571-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333571
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333571
    reference: chr 10
allele count: 2
allele frequency: 1.6619025460347e-5
allele num: 120344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.637A>G
  hgvsp: ENSP00000363881.3:p.Thr213Ala
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.637A>G
  hgvsp: ENSP00000363883.3:p.Thr213Ala
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.637A>G
  hgvsp: ENSP00000414095.1:p.Thr213Ala
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*320A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.637A>G
  hgvsp: ENSP00000363878.1:p.Thr213Ala
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.637A>G
  hgvsp: ENSP00000363880.1:p.Thr213Ala
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.637A>G
  hgvsp: ENSP00000363874.1:p.Thr213Ala
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.694A>G
  hgvsp: ENSP00000444856.1:p.Thr232Ala
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.466A>G
  hgvsp: ENSP00000473659.1:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr232Ala
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

10-35333578-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333578
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333578
    reference: chr 10
allele count: 1
allele frequency: 8.311999202048076e-6
allele num: 120308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.630C>T
  hgvsp: ENST00000421317.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.687C>T
  hgvsp: ENST00000537177.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.630C>T
  hgvsp: ENST00000374742.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.630C>T
  hgvsp: ENST00000374748.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.630C>T
  hgvsp: ENST00000374746.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.459C>T
  hgvsp: ENST00000602371.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.630C>T
  hgvsp: ENST00000374749.3:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*313C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.630C>T
  hgvsp: ENST00000374751.3:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro229Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

10-35333580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333580
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333580
    reference: chr 10
allele count: 1
allele frequency: 8.312413758707254e-6
allele num: 120302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.457C>T
  hgvsp: ENSP00000473659.1:p.Pro153Ser
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.628C>T
  hgvsp: ENSP00000363880.1:p.Pro210Ser
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.628C>T
  hgvsp: ENSP00000363878.1:p.Pro210Ser
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.628C>T
  hgvsp: ENSP00000414095.1:p.Pro210Ser
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.628C>T
  hgvsp: ENSP00000363874.1:p.Pro210Ser
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.628C>T
  hgvsp: ENSP00000363881.3:p.Pro210Ser
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.685C>T
  hgvsp: ENSP00000444856.1:p.Pro229Ser
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.628C>T
  hgvsp: ENSP00000363883.3:p.Pro210Ser
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*311C>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro229Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

10-35333607-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333607
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333607
    reference: chr 10
allele count: 1
allele frequency: 8.334027835652971e-6
allele num: 119990
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.661-3C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.604-3C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.433-3C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.604-3C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*287-3C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.604-3C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.604-3C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.604-3C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.604-3C>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
hgvs: c.661-3C>T
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: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

10-35333623-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333623
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333623
    reference: chr 10
allele count: 12
allele frequency: 1.001953809929362e-4
allele num: 119766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.604-19A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.604-19A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.661-19A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.604-19A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.604-19A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.604-19A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.433-19A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*287-19A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.604-19A>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12641
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34329
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

10-35333638-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333638
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333638
    reference: chr 10
allele count: 1
allele frequency: 8.362322718758362e-6
allele num: 119584
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.604-34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.604-34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.604-34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.433-34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.661-34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.604-34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.604-34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*287-34A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.604-34A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39502
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

10-35333639-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333639
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333639
    reference: chr 10
allele count: 7
allele frequency: 5.853625903130854e-5
allele num: 119584
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.604-35A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.433-35A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*287-35A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.661-35A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.604-35A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.604-35A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.604-35A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.604-35A>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.604-35A>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13022
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4775
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

10-35333647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333647
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333647
    reference: chr 10
allele count: 2
allele frequency: 1.673248109229637e-5
allele num: 119528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.604-43C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.604-43C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.604-43C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*287-43C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.604-43C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.661-43C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.604-43C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.604-43C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.433-43C>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

10-35333648-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333648
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333648
    reference: chr 10
allele count: 1
allele frequency: 8.368340892734607e-6
allele num: 119498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.604-44G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*287-44G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.604-44G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.604-44G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.604-44G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.604-44G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.661-44G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.433-44G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.604-44G>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13538
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39851
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

10-35333649-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333649
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333649
    reference: chr 10
allele count: 1
allele frequency: 8.363022061652199e-6
allele num: 119574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.433-45T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.604-45T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.661-45T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.604-45T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.604-45T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*287-45T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.604-45T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.604-45T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.604-45T>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33596
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

10-35333668-CTGAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333668
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333664
    reference: chr 10
allele count: 1
allele frequency: 8.348499774590506e-6
allele num: 119782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.603+28_603+31delATCA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.603+28_603+31delATCA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.603+28_603+31delATCA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.660+28_660+31delATCA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.603+28_603+31delATCA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.603+28_603+31delATCA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.432+28_432+31delATCA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*286+28_*286+31delATCA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.603+28_603+31delATCA
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3299
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1590
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: CTGAT
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

10-35333673-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333673
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333673
    reference: chr 10
allele count: 1
allele frequency: 8.333472224537076e-6
allele num: 119998
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.603+27A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.432+27A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.603+27A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.660+27A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*286+27A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.603+27A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.603+27A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.603+27A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.603+27A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: T
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

10-35333688-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333688
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333688
    reference: chr 10
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.603+12C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.603+12C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.603+12C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*286+12C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.432+12C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.603+12C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.603+12C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.603+12C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.660+12C>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-35333695-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333695
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333695
    reference: chr 10
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*286+5A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.603+5A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.660+5A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.432+5A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.603+5A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.603+5A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.603+5A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.603+5A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.603+5A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
hgvs: c.660+5A>G
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

10-35333711-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333711
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333712
    reference: chr 10
allele count: 1
allele frequency: 8.263097008758882e-6
allele num: 121020
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.591dupA
  hgvsp: ENSP00000363881.3:p.Phe198IlefsTer11
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.420dupA
  hgvsp: ENSP00000473659.1:p.Phe141IlefsTer11
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.648dupA
  hgvsp: ENSP00000444856.1:p.Phe217IlefsTer11
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.591dupA
  hgvsp: ENSP00000363883.3:p.Phe198IlefsTer11
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.591dupA
  hgvsp: ENSP00000363880.1:p.Phe198IlefsTer11
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*274dupA
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.591dupA
  hgvsp: ENSP00000363878.1:p.Phe198IlefsTer11
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.591dupA
  hgvsp: ENSP00000414095.1:p.Phe198IlefsTer11
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.591dupA
  hgvsp: ENSP00000363874.1:p.Phe198IlefsTer11
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe217IlefsTer11
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

10-35333726-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333726
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333726
    reference: chr 10
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.577C>A
  hgvsp: ENSP00000414095.1:p.Gln193Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*260C>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.577C>A
  hgvsp: ENSP00000363880.1:p.Gln193Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.634C>A
  hgvsp: ENSP00000444856.1:p.Gln212Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.577C>A
  hgvsp: ENSP00000363874.1:p.Gln193Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.577C>A
  hgvsp: ENSP00000363881.3:p.Gln193Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.577C>A
  hgvsp: ENSP00000363883.3:p.Gln193Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.406C>A
  hgvsp: ENSP00000473659.1:p.Gln136Lys
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.577C>A
  hgvsp: ENSP00000363878.1:p.Gln193Lys
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3303
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln212Lys
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/10-35333731-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333731
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333731
    reference: chr 10
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.572T>G
  hgvsp: ENSP00000363880.1:p.Val191Gly
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.401T>G
  hgvsp: ENSP00000473659.1:p.Val134Gly
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.572T>G
  hgvsp: ENSP00000363874.1:p.Val191Gly
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.629T>G
  hgvsp: ENSP00000444856.1:p.Val210Gly
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.572T>G
  hgvsp: ENSP00000414095.1:p.Val191Gly
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.572T>G
  hgvsp: ENSP00000363883.3:p.Val191Gly
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.572T>G
  hgvsp: ENSP00000363881.3:p.Val191Gly
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.572T>G
  hgvsp: ENSP00000363878.1:p.Val191Gly
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*255T>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3303
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46894
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5315
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val210Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

10-35333734-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333734
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333734
    reference: chr 10
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.569A>G
  hgvsp: ENSP00000363878.1:p.His190Arg
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.569A>G
  hgvsp: ENSP00000363874.1:p.His190Arg
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.569A>G
  hgvsp: ENSP00000363880.1:p.His190Arg
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.569A>G
  hgvsp: ENSP00000363883.3:p.His190Arg
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.569A>G
  hgvsp: ENSP00000363881.3:p.His190Arg
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.569A>G
  hgvsp: ENSP00000414095.1:p.His190Arg
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*252A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.398A>G
  hgvsp: ENSP00000473659.1:p.His133Arg
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.626A>G
  hgvsp: ENSP00000444856.1:p.His209Arg
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His209Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

10-35333739-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333739
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333739
    reference: chr 10
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*247T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.564T>C
  hgvsp: ENST00000421317.1:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.564T>C
  hgvsp: ENST00000374749.3:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.621T>C
  hgvsp: ENST00000537177.1:c.621T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.564T>C
  hgvsp: ENST00000374751.3:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.564T>C
  hgvsp: ENST00000374748.1:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.564T>C
  hgvsp: ENST00000374746.1:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.393T>C
  hgvsp: ENST00000602371.1:c.393T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.564T>C
  hgvsp: ENST00000374742.1:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46931
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe207Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-35333748-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333748
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333748
    reference: chr 10
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.555T>G
  hgvsp: ENSP00000363881.3:p.Ile185Met
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.612T>G
  hgvsp: ENSP00000444856.1:p.Ile204Met
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.384T>G
  hgvsp: ENSP00000473659.1:p.Ile128Met
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.555T>G
  hgvsp: ENSP00000363880.1:p.Ile185Met
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*238T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.555T>G
  hgvsp: ENSP00000363874.1:p.Ile185Met
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.555T>G
  hgvsp: ENSP00000363883.3:p.Ile185Met
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.555T>G
  hgvsp: ENSP00000414095.1:p.Ile185Met
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.555T>G
  hgvsp: ENSP00000363878.1:p.Ile185Met
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile204Met
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

10-35333784-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333784
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333784
    reference: chr 10
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.519A>T
  hgvsp: ENST00000374748.1:c.519A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.348A>T
  hgvsp: ENST00000602371.1:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.519A>T
  hgvsp: ENST00000374746.1:c.519A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.519A>T
  hgvsp: ENST00000374751.3:c.519A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.519A>T
  hgvsp: ENST00000374749.3:c.519A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.519A>T
  hgvsp: ENST00000421317.1:c.519A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*202A>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.576A>T
  hgvsp: ENST00000537177.1:c.576A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.519A>T
  hgvsp: ENST00000374742.1:c.519A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly192Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

10-35333803-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333803
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333803
    reference: chr 10
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-7G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-7G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-7G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-7G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-7G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-7G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-7G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-7G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-7G>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
hgvs: c.564-7G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

10-35333807-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333807
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333807
    reference: chr 10
allele count: 1
allele frequency: 8.292699107705576e-6
allele num: 120588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-11C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-11C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-11C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-11C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-11C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-11C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-11C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-11C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-11C>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5119
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45245
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

10-35333809-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333809
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333809
    reference: chr 10
allele count: 7
allele frequency: 5.81182956394673e-5
allele num: 120444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-13T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-13T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-13T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-13T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-13T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-13T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-13T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-13T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-13T>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15888
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

10-35333811-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333811
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333811
    reference: chr 10
allele count: 2
allele frequency: 1.660688189185599e-5
allele num: 120432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-15T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-15T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-15T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-15T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-15T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-15T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-15T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-15T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-15T>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

10-35333813-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333813
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333813
    reference: chr 10
allele count: 1
allele frequency: 8.307855908547122e-6
allele num: 120368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-17G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-17G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-17G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-17G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-17G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-17G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-17G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-17G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-17G>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3303
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

10-35333815-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333815
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333815
    reference: chr 10
allele count: 6
allele frequency: 4.989356040447046e-5
allele num: 120256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-19G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-19G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-19G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-19G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-19G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-19G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-19G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-19G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-19G>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15655
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4969
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-35333834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333834
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333834
    reference: chr 10
allele count: 2
allele frequency: 1.676755143446403e-5
allele num: 119278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-38G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-38G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-38G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-38G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-38G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-38G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-38G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-38G>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-38G>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25510
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4361
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

10-35333845-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333845
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333845
    reference: chr 10
allele count: 1
allele frequency: 8.467687305243193e-6
allele num: 118096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-49A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-49A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-49A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-49A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-49A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-49A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-49A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-49A>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-49A>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11069
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5140
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-35333846-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35333846
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35333846
    reference: chr 10
allele count: 1
allele frequency: 8.509479560230096e-6
allele num: 117516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*190-50C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.507-50C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.507-50C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.564-50C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.507-50C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.336-50C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.507-50C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.507-50C>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.507-50C>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2369
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3037
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5518
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/10-35338564-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35338564
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35338564
    reference: chr 10
allele count: 1
allele frequency: 9.718172983479106e-6
allele num: 102900
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.563+47T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.506+47T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.506+47T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.506+47T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.506+47T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.506+47T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*189+47T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.506+47T>G
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.335+47T>G
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4678
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5899
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11873
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

10-35338568-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35338568
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35338568
    reference: chr 10
allele count: 1
allele frequency: 9.689734695064048e-6
allele num: 103202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.506+43T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.506+43T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*189+43T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.563+43T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.506+43T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.506+43T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.506+43T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.335+43T>A
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.506+43T>A
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7791
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

10-35338569-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35338569
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35338569
    reference: chr 10
allele count: 1
allele frequency: 9.683166782864668e-6
allele num: 103272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*189+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.506+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.506+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.335+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.563+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.506+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.506+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.506+42T>C
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.506+42T>C
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16023
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2415
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3301
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5445
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-35338584-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35338584
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 35338584
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 105628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363883
  ensembl transcript: ENST00000374751
  gene symbol: CUL2
  hgvsc: ENST00000374751.3:c.506+27G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363886
  ensembl transcript: ENST00000374754
  gene symbol: CUL2
  hgvsc: ENST00000374754.4:c.*189+27G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000444856
  ensembl transcript: ENST00000537177
  gene symbol: CUL2
  hgvsc: ENST00000537177.1:c.563+27G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000473659
  ensembl transcript: ENST00000602371
  gene symbol: CUL2
  hgvsc: ENST00000602371.1:c.335+27G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363880
  ensembl transcript: ENST00000374748
  gene symbol: CUL2
  hgvsc: ENST00000374748.1:c.506+27G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363881
  ensembl transcript: ENST00000374749
  gene symbol: CUL2
  hgvsc: ENST00000374749.3:c.506+27G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363878
  ensembl transcript: ENST00000374746
  gene symbol: CUL2
  hgvsc: ENST00000374746.1:c.506+27G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000363874
  ensembl transcript: ENST00000374742
  gene symbol: CUL2
  hgvsc: ENST00000374742.1:c.506+27G>T
  variant of: http://identifiers.org/hgnc/2552
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108094
  ensembl protein: ENSP00000414095
  ensembl transcript: ENST00000421317
  gene symbol: CUL2
  hgvsc: ENST00000421317.1:c.506+27G>T
  variant of: http://identifiers.org/hgnc/2552
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8157
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4711
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 312
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10790
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56940
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.53765690376569e-5
allele num: 15296
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.413485e6

FS
type: SiteQuality
SIO_000300: 1.292e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.391e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.755802928679285e-5
allele num: 56954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6152
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.112e-1

FS
type: SiteQuality
SIO_000300: 6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.043e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

MQ
type: SiteQuality
SIO_000300: 5.885e1

DP
type: SiteQuality
SIO_000300: 1.413435e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9200
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.576351440220966e-5
allele num: 15206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56282
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.73e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 1.623e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e0

QD
type: SiteQuality
SIO_000300: 1.294e1

DP
type: SiteQuality
SIO_000300: 1.400628e6

GenotypeQuality
all individuals: 265
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variant carriers: 0

GenotypeQuality
all individuals: 341
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variant carriers: 0

GenotypeQuality
all individuals: 374
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variant carriers: 0

GenotypeQuality
all individuals: 172
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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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 145
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GenotypeQuality
all individuals: 2775
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.802126509280952e-5
allele num: 55490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15020
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.386146048432514e-5
allele num: 10654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.097e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

DP
type: SiteQuality
SIO_000300: 1.379989e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

FS
type: SiteQuality
SIO_000300: 5.282e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 510
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.895590855669712e-5
allele num: 52754
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5976
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.352e0

FS
type: SiteQuality
SIO_000300: 3.821e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e-1

QD
type: SiteQuality
SIO_000300: 1.08e1

MQ
type: SiteQuality
SIO_000300: 5.915e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 1.305204e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 1762
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variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

Latino
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: 758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8026
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.263467632412856e-4
allele num: 8836
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

DP
type: SiteQuality
SIO_000300: 1.271426e6

FS
type: SiteQuality
SIO_000300: 4.939e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.057e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.997842330283294e-5
allele num: 50054
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13046
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.409e1

MQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.211463e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2846
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.095557418273261e-5
allele num: 47720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5756
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.297e0

DP
type: SiteQuality
SIO_000300: 1.108273e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.586e0

QD
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 9.347e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 3.388e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e0

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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bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.111932418162619e-5
allele num: 47350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 700
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.199e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQ
type: SiteQuality
SIO_000300: 3.36e1

QD
type: SiteQuality
SIO_000300: 2.07e0

DP
type: SiteQuality
SIO_000300: 1.101145e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.393e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.257e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5560
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.790178571428571e-4
allele num: 7168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.599999999999999e-2

DP
type: SiteQuality
SIO_000300: 9.73943e5

ClippingRankSum
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SIO_000300: -1.278e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-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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bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9134
num of homozygotes: 0

European (Non-Finnish)
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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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allele count: 0
allele frequency: 0.0e0
allele num: 5562
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

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

East Asian
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allele frequency: 1.399776035834267e-4
allele num: 7144
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 9.6989e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.392e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

Other
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allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7092
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5528
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9058
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 42588
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.918666931164451e-5
allele num: 10082
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.54e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.774e0

QD
type: SiteQuality
SIO_000300: 2.807e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.011e0

DP
type: SiteQuality
SIO_000300: 9.61864e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.26e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.388458966274959e-5
allele num: 41868
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8948
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.289e1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 3.424e0

DP
type: SiteQuality
SIO_000300: 9.56085e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41028
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.48954e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.047e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.199999999999999e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5440
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9384
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40284
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.151543067710732e-4
allele num: 8684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7578
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
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VQSLOD
type: SiteQuality
SIO_000300: 4.49e0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.46093e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52940
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6194
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 3.766194636938837e-4
allele num: 13276
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 7214
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.159768e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.156e1

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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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52938
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6192
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South Asian
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allele count: 0
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African
type: Population
allele count: 1
allele frequency: 1.130198915009042e-4
allele num: 8848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.128e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.318e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.162337e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 476
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
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African
type: Population
allele count: 2
allele frequency: 2.252252252252252e-4
allele num: 8880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13326
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6206
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7210
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.765e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

DP
type: SiteQuality
SIO_000300: 1.186421e6

FS
type: SiteQuality
SIO_000300: 2.718e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.451e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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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bin: 1.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7232
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.033760423022168e-4
allele num: 9834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.191468e6

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.872308556450103e-5
allele num: 53410
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.191468e6

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.851029172219754e-5
allele num: 54024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13626
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
SIO_000300: 1.25002e6

VQSLOD
type: SiteQuality
SIO_000300: -1.549e0

MQ
type: SiteQuality
SIO_000300: 5.846e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e-1

FS
type: SiteQuality
SIO_000300: 5.839e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.248e0

MQRankSum
type: SiteQuality
SIO_000300: -1.49e-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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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9028
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13658
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.840264998159735e-5
allele num: 54340
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.896e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.048e1

DP
type: SiteQuality
SIO_000300: 1.285295e6

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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.62621024767016e-5
allele num: 55154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.195e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
SIO_000300: 4.363e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.37e-1

DP
type: SiteQuality
SIO_000300: 1.323249e6

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14048
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.319957761351637e-4
allele num: 7576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56174
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.19e-1

QD
type: SiteQuality
SIO_000300: 1.507e1

DP
type: SiteQuality
SIO_000300: 1.359391e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e0

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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.7481906227055e-5
allele num: 57202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.367e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.363e0

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

DP
type: SiteQuality
SIO_000300: 1.394607e6

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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bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9340
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.72717537738782e-5
allele num: 57898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

QD
type: SiteQuality
SIO_000300: 1.456e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.415565e6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.704448610874382e-5
allele num: 58670
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
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East Asian
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.911e1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

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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bin: 9.75e1
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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: 7912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.083539499101908e-5
allele num: 59014
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10748
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14590
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
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QD
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FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -4.64e-1

BaseQRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10814
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59528
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.056635672020287e-4
allele num: 9464
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14694
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.439e0

MQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.219e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: 4.64e-1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10898
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14854
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.660798511924533e-5
allele num: 60212
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8070
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.177e1

VQSLOD
type: SiteQuality
SIO_000300: -2.604e0

FS
type: SiteQuality
SIO_000300: 3.198e0

MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.894e0

DP
type: SiteQuality
SIO_000300: 1.466538e6

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15050
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.639989504067174e-5
allele num: 60976
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10988
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.479404e6

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

FS
type: SiteQuality
SIO_000300: 6.791e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-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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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15522
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.592610288262462e-5
allele num: 62790
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.518734e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.4e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.587e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-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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bin: 9.75e1
variant carriers: 1

Latino
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allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65794
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

FS
type: SiteQuality
SIO_000300: 3.017e0

DP
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 5.858e1

ClippingRankSum
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SIO_000300: -1.263e0

MQRankSum
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QD
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SIO_000300: 1.861e1

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

Latino
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allele count: 3
allele frequency: 2.604166666666667e-4
allele num: 11520
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66172
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.01e-1

ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -9.44e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
type: Population
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allele frequency: 9.871668311944718e-5
allele num: 10130
num of homozygotes: 0

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

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

Latino
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allele count: 0
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allele num: 11522
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

VQSLOD
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.955e1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.584956e6

QD
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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GenotypeQuality
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GenotypeQuality
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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: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510665296996797e-5
allele num: 66196
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

Latino
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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: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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DP
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.543e0

MQRankSum
type: SiteQuality
SIO_000300: -1.981e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
all individuals: 707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3300
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.978239366963402e-4
allele num: 10110
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66184
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.438e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.582214e6

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 44964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 513
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variant carriers: 0

GenotypeQuality
all individuals: 5250
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511395925276585e-5
allele num: 66164
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.580315e6

FS
type: SiteQuality
SIO_000300: 2.536e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.99e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

VQSLOD
type: SiteQuality
SIO_000300: 8.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.385e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.5e0
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GenotypeQuality
all individuals: 16
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 368
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variant carriers: 0

GenotypeQuality
all individuals: 3300
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511487303506651e-5
allele num: 66160
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: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.373e1

DP
type: SiteQuality
SIO_000300: 1.579378e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.567e0

MQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.71e-1

FS
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 96
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 3.75e1
variant carriers: 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: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.090875867949811e-5
allele num: 16418
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.085e-1

DP
type: SiteQuality
SIO_000300: 1.566498e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.133e0

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.556e0

GenotypeQuality
all individuals: 4959
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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
all individuals: 1275
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GenotypeQuality
all individuals: 241
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GenotypeQuality
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GenotypeQuality
all individuals: 3309
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variant carriers: 12

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 977
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variant carriers: 0

GenotypeQuality
all individuals: 1315
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variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.951340615690168e-4
allele num: 10070
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: 902
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.35085276714236e-4
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65826
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.557301e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.69e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

QD
type: SiteQuality
SIO_000300: 1.409e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

GenotypeQuality
all individuals: 789
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 513
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GenotypeQuality
all individuals: 343
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.700191404210893e-5
allele num: 11494
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.002e0

QD
type: SiteQuality
SIO_000300: 1.802e1

FS
type: SiteQuality
SIO_000300: 1.5985e1

VQSLOD
type: SiteQuality
SIO_000300: -1.902e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

DP
type: SiteQuality
SIO_000300: 1.559037e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e0

GenotypeQuality
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bin: 7.75e1
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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GenotypeQuality
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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: 3305
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 331
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 6.951340615690168e-4
allele num: 10070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65712
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

DP
type: SiteQuality
SIO_000300: 1.559255e6

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 8.08e0

QD
type: SiteQuality
SIO_000300: 1.634e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.93e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 992
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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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
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variant carriers: 0

GenotypeQuality
all individuals: 1568
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variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045901739209893e-5
allele num: 65662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 1.56571e6

VQSLOD
type: SiteQuality
SIO_000300: -1.91e0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

FS
type: SiteQuality
SIO_000300: 1.4482e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.381e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.374e0

GenotypeQuality
all individuals: 1571
bin: 7.75e1
variant carriers: 0

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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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 849
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 965
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GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3298
bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 1
allele frequency: 6.109481915933529e-5
allele num: 16368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65676
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.116e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 1.485e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.567623e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.371e0

QD
type: SiteQuality
SIO_000300: 7.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.708e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.188777936281503e-4
allele num: 8412
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

FS
type: SiteQuality
SIO_000300: 1.81e0

QD
type: SiteQuality
SIO_000300: 1.577e1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.07e-2

DP
type: SiteQuality
SIO_000300: 1.567326e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.27e-1

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

GenotypeQuality
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variant carriers: 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: 10148
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65834
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

MQ
type: SiteQuality
SIO_000300: 5.747e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.93e-1

QD
type: SiteQuality
SIO_000300: 1.014e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

DP
type: SiteQuality
SIO_000300: 1.593506e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.88e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515978412467406e-5
allele num: 65964
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
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: 10166
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.493e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: -7.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

FS
type: SiteQuality
SIO_000300: 3.274e0

VQSLOD
type: SiteQuality
SIO_000300: -1.854e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

DP
type: SiteQuality
SIO_000300: 1.59939e6

GenotypeQuality
all individuals: 163
bin: 3.75e1
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
all individuals: 5176
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50879628232596e-5
allele num: 66278
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.616888e6

FS
type: SiteQuality
SIO_000300: 2.907e0

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

QD
type: SiteQuality
SIO_000300: 2.793e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.089e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505525277769414e-5
allele num: 66422
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.397e0

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.437e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 1.622268e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

QD
type: SiteQuality
SIO_000300: 1.411e1

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
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
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e0

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.823e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.627887e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.85e-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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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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DP
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 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: 16498
num of homozygotes: 0

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

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

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

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

VQSLOD
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SIO_000300: 4.19e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

DP
type: SiteQuality
SIO_000300: 1.630443e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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
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GenotypeQuality
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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: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
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: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.512e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

FS
type: SiteQuality
SIO_000300: 4.746e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 1.630663e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.630827e6

FS
type: SiteQuality
SIO_000300: 5.922e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.684e1

MQRankSum
type: SiteQuality
SIO_000300: 5.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.25e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.761e0

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.631021e6

QD
type: SiteQuality
SIO_000300: 1.239e1

MQ
type: SiteQuality
SIO_000300: 5.916e1

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: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.551e0

QD
type: SiteQuality
SIO_000300: 1.288e1

FS
type: SiteQuality
SIO_000300: 2.815e0

MQRankSum
type: SiteQuality
SIO_000300: -1.227e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.397e0

VQSLOD
type: SiteQuality
SIO_000300: -4.785e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e0

DP
type: SiteQuality
SIO_000300: 1.628898e6

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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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.69e-1

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 7.456e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.616467e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

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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bin: 7.75e1
variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507886245061673e-5
allele num: 66318
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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African
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Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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Latino
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allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

FS
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66232
num of homozygotes: 0

Other
type: Population
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allele num: 900
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South Asian
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allele count: 7
allele frequency: 4.279251742266781e-4
allele num: 16358
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

European (Non-Finnish)
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allele count: 2
allele frequency: 3.020144362900547e-5
allele num: 66222
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

South Asian
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 3.44e0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16338
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: 11522
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510847887834653e-5
allele num: 66188
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.957e0

InbreedingCoeff
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SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 2.582e0

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 3.45e-1

ReadPosRankSum
type: SiteQuality
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DP
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SIO_000300: 1.600924e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.523e1

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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bin: 1.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.926958570587081e-4
allele num: 10186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512493193780628e-5
allele num: 66116
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.18e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.36e-1

DP
type: SiteQuality
SIO_000300: 1.594942e6

VQSLOD
type: SiteQuality
SIO_000300: 8.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.004e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.454e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.04905936518584e-5
allele num: 65594
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.610000000000001e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.101e0

DP
type: SiteQuality
SIO_000300: 1.498479e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 1.903e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.046e1

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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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.241418050181001e-5
allele num: 16022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.195e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.466473e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

VQSLOD
type: SiteQuality
SIO_000300: -2.361e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.277463904582549e-5
allele num: 15930
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.222e0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.34e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.467491e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.285e0

GenotypeQuality
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bin: 2.75e1
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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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 55372
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.118067978533095e-4
allele num: 8944
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5918
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

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

South Asian
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
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MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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SIO_000300: 4.028e0

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5928
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9892
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.800374477891401e-5
allele num: 55544
num of homozygotes: 0

South Asian
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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BaseQRankSum
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

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

Other
type: Population
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num of homozygotes: 0

African
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.798755261359139e-5
allele num: 55594
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQRankSum
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ClippingRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6026
num of homozygotes: 0

Other
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57072
num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

QD
type: SiteQuality
SIO_000300: 2.26e0

DP
type: SiteQuality
SIO_000300: 1.428264e6