11-18586461-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586461
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586461
    reference: chr 11
allele count: 10
allele frequency: 8.240083060037245e-5
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*228G>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.290G>C
  hgvsp: ENSP00000437538.1:p.Cys97Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.590G>C
  hgvsp: ENSP00000442974.1:p.Cys197Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.524G>C
  hgvsp: ENSP00000368697.4:p.Cys175Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.590G>C
  hgvsp: ENSP00000379500.2:p.Cys197Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.532G>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.476G>C
  hgvsp: ENSP00000441092.1:p.Cys159Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.524G>C
  hgvsp: ENSP00000323353.6:p.Cys175Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.590G>C
  hgvsp: ENSP00000300038.7:p.Cys197Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.361G>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys197Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

11-18586462-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586462
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586462
    reference: chr 11
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*227T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.589T>A
  hgvsp: ENSP00000300038.7:p.Cys197Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.523T>A
  hgvsp: ENSP00000368697.4:p.Cys175Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.589T>A
  hgvsp: ENSP00000379500.2:p.Cys197Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.531T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.589T>A
  hgvsp: ENSP00000442974.1:p.Cys197Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.523T>A
  hgvsp: ENSP00000323353.6:p.Cys175Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.475T>A
  hgvsp: ENSP00000441092.1:p.Cys159Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.289T>A
  hgvsp: ENSP00000437538.1:p.Cys97Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.360T>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8747
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys197Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

11-18586463-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586463
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586463
    reference: chr 11
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.288C>T
  hgvsp: ENST00000541984.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.522C>T
  hgvsp: ENST00000320750.6:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.474C>T
  hgvsp: ENST00000535484.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.588C>T
  hgvsp: ENST00000300038.7:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.359C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*226C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.522C>T
  hgvsp: ENST00000379387.4:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.588C>T
  hgvsp: ENST00000396197.3:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.588C>T
  hgvsp: ENST00000543987.1:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.530C>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1658
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3113
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala196Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP

11-18586463-G-GAAATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586463
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586468
    reference: chr 11
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: GAAATT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*225_*226insAATTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.587_588insAATTT
  hgvsp: ENSP00000300038.7:p.Cys197IlefsTer5
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.521_522insAATTT
  hgvsp: ENSP00000323353.6:p.Cys175IlefsTer5
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.587_588insAATTT
  hgvsp: ENSP00000379500.2:p.Cys197IlefsTer5
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.287_288insAATTT
  hgvsp: ENSP00000437538.1:p.Cys97IlefsTer5
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.358_359insAATTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.587_588insAATTT
  hgvsp: ENSP00000442974.1:p.Cys197IlefsTer5
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.521_522insAATTT
  hgvsp: ENSP00000368697.4:p.Cys175IlefsTer5
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.473_474insAATTT
  hgvsp: ENSP00000441092.1:p.Cys159IlefsTer5
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.529_530insAATTT
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys197IlefsTer5
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

11-18586472-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586472
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586472
    reference: chr 11
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.350C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.579C>T
  hgvsp: ENST00000396197.3:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.513C>T
  hgvsp: ENST00000379387.4:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.579C>T
  hgvsp: ENST00000300038.7:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.513C>T
  hgvsp: ENST00000320750.6:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*217C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.579C>T
  hgvsp: ENST00000543987.1:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.279C>T
  hgvsp: ENST00000541984.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.465C>T
  hgvsp: ENST00000535484.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.521C>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu193Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

11-18586482-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586482
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586482
    reference: chr 11
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.503G>A
  hgvsp: ENSP00000323353.6:p.Gly168Asp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.569G>A
  hgvsp: ENSP00000379500.2:p.Gly190Asp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.503G>A
  hgvsp: ENSP00000368697.4:p.Gly168Asp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.269G>A
  hgvsp: ENSP00000437538.1:p.Gly90Asp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.455G>A
  hgvsp: ENSP00000441092.1:p.Gly152Asp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.569G>A
  hgvsp: ENSP00000300038.7:p.Gly190Asp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.569G>A
  hgvsp: ENSP00000442974.1:p.Gly190Asp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.511G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*207G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.340G>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly190Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

11-18586488-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586488
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586488
    reference: chr 11
allele count: 3
allele frequency: 2.47239162683369e-5
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.497T>C
  hgvsp: ENSP00000323353.6:p.Val166Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.563T>C
  hgvsp: ENSP00000442974.1:p.Val188Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.263T>C
  hgvsp: ENSP00000437538.1:p.Val88Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.563T>C
  hgvsp: ENSP00000379500.2:p.Val188Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.334T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.563T>C
  hgvsp: ENSP00000300038.7:p.Val188Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.497T>C
  hgvsp: ENSP00000368697.4:p.Val166Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*201T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.449T>C
  hgvsp: ENSP00000441092.1:p.Val150Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.505T>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val188Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

11-18586490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586490
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586490
    reference: chr 11
allele count: 8
allele frequency: 6.593696426216537e-5
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.503G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.332G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.561G>A
  hgvsp: ENST00000300038.7:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.447G>A
  hgvsp: ENST00000535484.1:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*199G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.495G>A
  hgvsp: ENST00000320750.6:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.495G>A
  hgvsp: ENST00000379387.4:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.561G>A
  hgvsp: ENST00000396197.3:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.261G>A
  hgvsp: ENST00000541984.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.561G>A
  hgvsp: ENST00000543987.1:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11061
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8715
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val187Val
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-18586493-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586493
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586493
    reference: chr 11
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.329T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.500T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.492T>C
  hgvsp: ENST00000320750.6:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.558T>C
  hgvsp: ENST00000396197.3:c.558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.558T>C
  hgvsp: ENST00000300038.7:c.558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.492T>C
  hgvsp: ENST00000379387.4:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.444T>C
  hgvsp: ENST00000535484.1:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.558T>C
  hgvsp: ENST00000543987.1:c.558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.258T>C
  hgvsp: ENST00000541984.1:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*196T>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr186Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

11-18586503-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586503
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586503
    reference: chr 11
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.482A>G
  hgvsp: ENSP00000323353.6:p.Asn161Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.434A>G
  hgvsp: ENSP00000441092.1:p.Asn145Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.248A>G
  hgvsp: ENSP00000437538.1:p.Asn83Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.548A>G
  hgvsp: ENSP00000379500.2:p.Asn183Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*186A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.482A>G
  hgvsp: ENSP00000368697.4:p.Asn161Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.548A>G
  hgvsp: ENSP00000442974.1:p.Asn183Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.319A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.548A>G
  hgvsp: ENSP00000300038.7:p.Asn183Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.490A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn183Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-18586546-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586546
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586546
    reference: chr 11
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*143A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.447A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.439A>G
  hgvsp: ENSP00000323353.6:p.Thr147Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.391A>G
  hgvsp: ENSP00000441092.1:p.Thr131Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.439A>G
  hgvsp: ENSP00000368697.4:p.Thr147Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.276A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.505A>G
  hgvsp: ENSP00000300038.7:p.Thr169Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.505A>G
  hgvsp: ENSP00000442974.1:p.Thr169Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.505A>G
  hgvsp: ENSP00000379500.2:p.Thr169Ala
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.205A>G
  hgvsp: ENSP00000437538.1:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr169Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-18586549-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586549
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586549
    reference: chr 11
allele count: 1
allele frequency: 8.288300235387727e-6
allele num: 120652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.502G>T
  hgvsp: ENSP00000442974.1:p.Asp168Tyr
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.502G>T
  hgvsp: ENSP00000379500.2:p.Asp168Tyr
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.273G>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.502G>T
  hgvsp: ENSP00000300038.7:p.Asp168Tyr
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.436G>T
  hgvsp: ENSP00000323353.6:p.Asp146Tyr
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.436G>T
  hgvsp: ENSP00000368697.4:p.Asp146Tyr
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*140G>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.202G>T
  hgvsp: ENSP00000437538.1:p.Asp68Tyr
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.388G>T
  hgvsp: ENSP00000441092.1:p.Asp130Tyr
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.444G>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp168Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-18586550-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586550
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586550
    reference: chr 11
allele count: 3
allele frequency: 2.486119167978785e-5
allele num: 120670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.435A>G
  hgvsp: ENST00000320750.6:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.435A>G
  hgvsp: ENST00000379387.4:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.387A>G
  hgvsp: ENST00000535484.1:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*139A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.272A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.501A>G
  hgvsp: ENST00000396197.3:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.201A>G
  hgvsp: ENST00000541984.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.501A>G
  hgvsp: ENST00000300038.7:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.501A>G
  hgvsp: ENST00000543987.1:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.443A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser167Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-18586569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586569
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586569
    reference: chr 11
allele count: 1
allele frequency: 8.392077878482712e-6
allele num: 119160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.265-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.380-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.494-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.428-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.436-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.428-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*132-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.494-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-12C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.494-12C>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-18586570-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586570
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586570
    reference: chr 11
allele count: 1
allele frequency: 8.400537634408602e-6
allele num: 119040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.380-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.494-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.494-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*132-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.436-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.265-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.428-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.494-13C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.428-13C>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40471
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3070
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

11-18586573-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586573
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586573
    reference: chr 11
allele count: 1
allele frequency: 8.444376889429329e-6
allele num: 118422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.436-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.494-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.380-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.265-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*132-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.428-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.428-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.494-16T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.494-16T>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.25e1
  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: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

11-18586582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586582
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586582
    reference: chr 11
allele count: 1
allele frequency: 8.54963920522554e-6
allele num: 116964
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.494-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.428-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.494-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*132-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.380-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.436-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.265-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.494-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-25C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.428-25C>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21710
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9391
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

11-18586587-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586587
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586587
    reference: chr 11
allele count: 1
allele frequency: 8.616678442793871e-6
allele num: 116054
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.494-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*132-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.428-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.265-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.494-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.436-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.494-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.380-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-30A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.428-30A>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

11-18586599-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586599
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586599
    reference: chr 11
allele count: 1
allele frequency: 8.872957001650369e-6
allele num: 112702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.380-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.494-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.436-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.494-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*132-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.428-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.494-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.428-42T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.265-42T>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6849
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12764
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5929
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

11-18586604-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18586604
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18586604
    reference: chr 11
allele count: 1
allele frequency: 9.115604091083115e-6
allele num: 109702
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*132-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.436-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.265-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.380-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.428-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.494-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.494-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.428-47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.494-47A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16625
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8804
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

11-18587847-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587847
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587847
    reference: chr 11
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.264+47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1290A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.493+47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*131+47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.427+47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.493+47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.493+47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.427+47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.435+47A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.379+47A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-18587856-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587856
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587857
    reference: chr 11
allele count: 6
allele frequency: 4.957612413861484e-5
allele num: 121026
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*131+37dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.264+37dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.493+37dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.493+37dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.435+37dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1300dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.379+37dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.427+37dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.427+37dupA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.493+37dupA
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

11-18587868-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587868
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587868
    reference: chr 11
allele count: 3
allele frequency: 2.47794627812469e-5
allele num: 121068
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*131+26T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.264+26T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.427+26T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.427+26T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1311T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.493+26T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.435+26T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.493+26T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.379+26T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.493+26T>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3705
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ

11-18587871-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587871
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587871
    reference: chr 11
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*131+23T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.379+23T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.264+23T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.493+23T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.493+23T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.427+23T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.427+23T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1314T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.493+23T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.435+23T>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

11-18587878-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587878
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587878
    reference: chr 11
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.493+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.379+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.264+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.427+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.493+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.427+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.435+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.493+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*131+16A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1321A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

11-18587887-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587887
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587887
    reference: chr 11
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.493+7A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.264+7A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.435+7A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.427+7A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.493+7A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1330A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.427+7A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.493+7A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*131+7A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.379+7A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
hgvs: c.493+7A>G
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

11-18587894-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587894
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587894
    reference: chr 11
allele count: 22
allele frequency: 1.814043998812626e-4
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.427G>A
  hgvsp: ENSP00000368697.4:p.Gly143Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.493G>A
  hgvsp: ENSP00000442974.1:p.Gly165Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1337G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.427G>A
  hgvsp: ENSP00000323353.6:p.Gly143Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.379G>A
  hgvsp: ENSP00000441092.1:p.Gly127Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.493G>A
  hgvsp: ENSP00000300038.7:p.Gly165Ser
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*131G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.435G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.264G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.493G>A
  hgvsp: ENSP00000379500.2:p.Gly165Ser
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly165Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

11-18587908-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587908
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587908
    reference: chr 11
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.250C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.479C>A
  hgvsp: ENSP00000442974.1:p.Ala160Glu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.413C>A
  hgvsp: ENSP00000368697.4:p.Ala138Glu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.421C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*117C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1351C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.479C>A
  hgvsp: ENSP00000300038.7:p.Ala160Glu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.413C>A
  hgvsp: ENSP00000323353.6:p.Ala138Glu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.479C>A
  hgvsp: ENSP00000379500.2:p.Ala160Glu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.365C>A
  hgvsp: ENSP00000441092.1:p.Ala122Glu
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2059
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala160Glu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-18587910-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587910
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587910
    reference: chr 11
allele count: 19
allele frequency: 1.565848030328004e-4
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1353T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.419T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.411T>G
  hgvsp: ENSP00000323353.6:p.Ile137Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.411T>G
  hgvsp: ENSP00000368697.4:p.Ile137Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.477T>G
  hgvsp: ENSP00000379500.2:p.Ile159Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*115T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.477T>G
  hgvsp: ENSP00000442974.1:p.Ile159Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.477T>G
  hgvsp: ENSP00000300038.7:p.Ile159Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.248T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.363T>G
  hgvsp: ENSP00000441092.1:p.Ile121Met
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile159Met
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: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

11-18587921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587921
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587921
    reference: chr 11
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.400C>T
  hgvsp: ENST00000379387.4:c.400C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.400C>T
  hgvsp: ENST00000320750.6:c.400C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.352C>T
  hgvsp: ENST00000535484.1:c.352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.466C>T
  hgvsp: ENST00000396197.3:c.466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.408C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*104C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.466C>T
  hgvsp: ENST00000543987.1:c.466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.237C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.466C>T
  hgvsp: ENST00000300038.7:c.466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1364C>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu156Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-18587921-G-GCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587921
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587923
    reference: chr 11
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: GCA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.398_399dupTG
  hgvsp: ENSP00000323353.6:p.Leu134CysfsTer2
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1366_194-1365dupTG
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.464_465dupTG
  hgvsp: ENSP00000379500.2:p.Leu156CysfsTer2
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.464_465dupTG
  hgvsp: ENSP00000442974.1:p.Leu156CysfsTer2
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.350_351dupTG
  hgvsp: ENSP00000441092.1:p.Leu118CysfsTer2
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.406_407dupTG
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.398_399dupTG
  hgvsp: ENSP00000368697.4:p.Leu134CysfsTer2
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.235_236dupTG
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.464_465dupTG
  hgvsp: ENSP00000300038.7:p.Leu156CysfsTer2
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*102_*103dupTG
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu156CysfsTer2
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-18587925-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587925
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587924
    reference: chr 11
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.461delA
  hgvsp: ENSP00000379500.2:p.Asp154AlafsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1369delA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.461delA
  hgvsp: ENSP00000300038.7:p.Asp154AlafsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.461delA
  hgvsp: ENSP00000442974.1:p.Asp154AlafsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.403delA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.395delA
  hgvsp: ENSP00000368697.4:p.Asp132AlafsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.232delA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.347delA
  hgvsp: ENSP00000441092.1:p.Asp116AlafsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.395delA
  hgvsp: ENSP00000323353.6:p.Asp132AlafsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*99delA
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp154AlafsTer3
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: GT
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-18587929-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587929
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587929
    reference: chr 11
allele count: 315
allele frequency: 2.642927860654775e-3
allele num: 119186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.229T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.392T>G
  hgvsp: ENSP00000323353.6:p.Val131Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.344T>G
  hgvsp: ENSP00000441092.1:p.Val115Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.400T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.458T>G
  hgvsp: ENSP00000442974.1:p.Val153Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*96T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.458T>G
  hgvsp: ENSP00000379500.2:p.Val153Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.392T>G
  hgvsp: ENSP00000368697.4:p.Val131Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.458T>G
  hgvsp: ENSP00000300038.7:p.Val153Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1372T>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 31487
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 10162
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 12443
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 42047
  bin: 6.25e1
  variant carriers: 9
hgvs: p.Val153Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

11-18587931-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587931
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587931
    reference: chr 11
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.456G>C
  hgvsp: ENSP00000442974.1:p.Gln152His
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.390G>C
  hgvsp: ENSP00000368697.4:p.Gln130His
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.456G>C
  hgvsp: ENSP00000379500.2:p.Gln152His
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*94G>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.390G>C
  hgvsp: ENSP00000323353.6:p.Gln130His
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.456G>C
  hgvsp: ENSP00000300038.7:p.Gln152His
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.342G>C
  hgvsp: ENSP00000441092.1:p.Gln114His
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1374G>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.398G>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.227G>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8498
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln152His
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-18587931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587931
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587931
    reference: chr 11
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.390G>A
  hgvsp: ENST00000379387.4:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.398G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.456G>A
  hgvsp: ENST00000396197.3:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*94G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.390G>A
  hgvsp: ENST00000320750.6:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.456G>A
  hgvsp: ENST00000543987.1:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.342G>A
  hgvsp: ENST00000535484.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.456G>A
  hgvsp: ENST00000300038.7:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1374G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.227G>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln152Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

11-18587936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587936
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587936
    reference: chr 11
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.451C>T
  hgvsp: ENSP00000300038.7:p.Arg151Trp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*89C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.451C>T
  hgvsp: ENSP00000379500.2:p.Arg151Trp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.337C>T
  hgvsp: ENSP00000441092.1:p.Arg113Trp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.385C>T
  hgvsp: ENSP00000368697.4:p.Arg129Trp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1379C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.385C>T
  hgvsp: ENSP00000323353.6:p.Arg129Trp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.451C>T
  hgvsp: ENSP00000442974.1:p.Arg151Trp
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.222C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.393C>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg151Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

11-18587940-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587940
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587940
    reference: chr 11
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1383G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.381G>A
  hgvsp: ENST00000379387.4:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.218G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.333G>A
  hgvsp: ENST00000535484.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*85G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.381G>A
  hgvsp: ENST00000320750.6:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.447G>A
  hgvsp: ENST00000396197.3:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.447G>A
  hgvsp: ENST00000300038.7:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.389G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.447G>A
  hgvsp: ENST00000543987.1:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2091
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu149Glu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

11-18587944-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587944
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587944
    reference: chr 11
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.385A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.443A>G
  hgvsp: ENSP00000442974.1:p.Asp148Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.443A>G
  hgvsp: ENSP00000379500.2:p.Asp148Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.329A>G
  hgvsp: ENSP00000441092.1:p.Asp110Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.377A>G
  hgvsp: ENSP00000368697.4:p.Asp126Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1387A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.443A>G
  hgvsp: ENSP00000300038.7:p.Asp148Gly
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*81A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.214A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.377A>G
  hgvsp: ENSP00000323353.6:p.Asp126Gly
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp148Gly
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

11-18587955-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587955
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587955
    reference: chr 11
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.318A>T
  hgvsp: ENST00000535484.1:c.318A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.374A>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.432A>T
  hgvsp: ENST00000543987.1:c.432A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.432A>T
  hgvsp: ENST00000396197.3:c.432A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.203A>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1398A>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.366A>T
  hgvsp: ENST00000320750.6:c.366A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.432A>T
  hgvsp: ENST00000300038.7:c.432A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.366A>T
  hgvsp: ENST00000379387.4:c.366A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*70A>T
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10522
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43329
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu144Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

11-18587956-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587956
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587956
    reference: chr 11
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.431T>C
  hgvsp: ENSP00000442974.1:p.Leu144Pro
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*69T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.365T>C
  hgvsp: ENSP00000368697.4:p.Leu122Pro
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.431T>C
  hgvsp: ENSP00000379500.2:p.Leu144Pro
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.373T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.202T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.317T>C
  hgvsp: ENSP00000441092.1:p.Leu106Pro
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.431T>C
  hgvsp: ENSP00000300038.7:p.Leu144Pro
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.365T>C
  hgvsp: ENSP00000323353.6:p.Leu122Pro
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1399T>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu144Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

11-18587959-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587959
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587959
    reference: chr 11
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.199C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.428C>T
  hgvsp: ENSP00000442974.1:p.Ser143Phe
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*66C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.370C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.428C>T
  hgvsp: ENSP00000379500.2:p.Ser143Phe
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.362C>T
  hgvsp: ENSP00000368697.4:p.Ser121Phe
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.428C>T
  hgvsp: ENSP00000300038.7:p.Ser143Phe
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1402C>T
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.314C>T
  hgvsp: ENSP00000441092.1:p.Ser105Phe
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.362C>T
  hgvsp: ENSP00000323353.6:p.Ser121Phe
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser143Phe
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-18587959-GAATAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587959
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587954
    reference: chr 11
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.423_427delGTATT
  hgvsp: ENSP00000300038.7:p.Met141IlefsTer6
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.423_427delGTATT
  hgvsp: ENSP00000442974.1:p.Met141IlefsTer6
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.194_198delGTATT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.357_361delGTATT
  hgvsp: ENSP00000323353.6:p.Met119IlefsTer6
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.365_369delGTATT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.357_361delGTATT
  hgvsp: ENSP00000368697.4:p.Met119IlefsTer6
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.423_427delGTATT
  hgvsp: ENSP00000379500.2:p.Met141IlefsTer6
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1407_194-1403delGTATT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.309_313delGTATT
  hgvsp: ENSP00000441092.1:p.Met103IlefsTer6
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*61_*65delGTATT
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Met141IlefsTer6
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: GAATAC
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD

11-18587963-A-ACATGGGAAGTTCCTCTTGAAACTTGGCAATCATTTCTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587963
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588001
    reference: chr 11
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: ACATGGGAAGTTCCTCTTGAAACTTGGCAATCATTTCTT
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsp: ENSP00000379500.2:p.Tyr142LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsp: ENSP00000368697.4:p.Tyr120LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsp: ENSP00000442974.1:p.Tyr142LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsp: ENSP00000300038.7:p.Tyr142LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsp: ENSP00000323353.6:p.Tyr120LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsp: ENSP00000441092.1:p.Tyr104LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10515
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr142LysfsTer3
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum

11-18587964-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587964
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587964
    reference: chr 11
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.357G>A
  hgvsp: ENSP00000368697.4:p.Met119Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.423G>A
  hgvsp: ENSP00000379500.2:p.Met141Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.423G>A
  hgvsp: ENSP00000442974.1:p.Met141Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.365G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1407G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.309G>A
  hgvsp: ENSP00000441092.1:p.Met103Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*61G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.423G>A
  hgvsp: ENSP00000300038.7:p.Met141Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.357G>A
  hgvsp: ENSP00000323353.6:p.Met119Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.194G>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8461
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Met141Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

11-18587966-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587966
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587966
    reference: chr 11
allele count: 14
allele frequency: 1.154030037753268e-4
allele num: 121314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.355A>C
  hgvsp: ENSP00000368697.4:p.Met119Leu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.363A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.421A>C
  hgvsp: ENSP00000442974.1:p.Met141Leu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.421A>C
  hgvsp: ENSP00000379500.2:p.Met141Leu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*59A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.192A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.355A>C
  hgvsp: ENSP00000323353.6:p.Met119Leu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1409A>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.307A>C
  hgvsp: ENSP00000441092.1:p.Met103Leu
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.421A>C
  hgvsp: ENSP00000300038.7:p.Met141Leu
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10507
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met141Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

11-18587976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587976
    reference: chr 11
allele count: 2
allele frequency: 1.649511744523621e-5
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.182G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.345G>A
  hgvsp: ENST00000379387.4:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.411G>A
  hgvsp: ENST00000396197.3:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.297G>A
  hgvsp: ENST00000535484.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1419G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.345G>A
  hgvsp: ENST00000320750.6:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.411G>A
  hgvsp: ENST00000300038.7:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.353G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*49G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.411G>A
  hgvsp: ENST00000543987.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43258
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu137Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

11-18587979-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587979
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587979
    reference: chr 11
allele count: 2
allele frequency: 1.649811096629436e-5
allele num: 121226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.350A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*46A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.294A>G
  hgvsp: ENST00000535484.1:c.294A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.342A>G
  hgvsp: ENST00000320750.6:c.342A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.408A>G
  hgvsp: ENST00000543987.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.342A>G
  hgvsp: ENST00000379387.4:c.342A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.408A>G
  hgvsp: ENST00000300038.7:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.408A>G
  hgvsp: ENST00000396197.3:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.179A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1422A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln136Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-18587980-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18587980
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587980
    reference: chr 11
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.341A>G
  hgvsp: ENSP00000323353.6:p.Gln114Arg
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.341A>G
  hgvsp: ENSP00000368697.4:p.Gln114Arg
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.407A>G
  hgvsp: ENSP00000442974.1:p.Gln136Arg
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.293A>G
  hgvsp: ENSP00000441092.1:p.Gln98Arg
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.407A>G
  hgvsp: ENSP00000379500.2:p.Gln136Arg
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.178A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1423A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*45A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.407A>G
  hgvsp: ENSP00000300038.7:p.Gln136Arg
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.349A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10452
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln136Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

11-18588000-TTTAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588000
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18587996
    reference: chr 11
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.317_320delTTAA
  hgvsp: ENSP00000368697.4:p.Ile106LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.154_157delTTAA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.325_328delTTAA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*21_*24delTTAA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.383_386delTTAA
  hgvsp: ENSP00000300038.7:p.Ile128LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.383_386delTTAA
  hgvsp: ENSP00000379500.2:p.Ile128LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1447_194-1444delTTAA
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.383_386delTTAA
  hgvsp: ENSP00000442974.1:p.Ile128LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.317_320delTTAA
  hgvsp: ENSP00000323353.6:p.Ile106LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.269_272delTTAA
  hgvsp: ENSP00000441092.1:p.Ile90LysfsTer3
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile128LysfsTer3
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: TTTAA
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

11-18588014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588014
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588014
    reference: chr 11
allele count: 1
allele frequency: 8.343206127250579e-6
allele num: 119858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.373G>A
  hgvsp: ENSP00000300038.7:p.Val125Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1457G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*11G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.373G>A
  hgvsp: ENSP00000442974.1:p.Val125Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.259G>A
  hgvsp: ENSP00000441092.1:p.Val87Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.307G>A
  hgvsp: ENSP00000368697.4:p.Val103Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.307G>A
  hgvsp: ENSP00000323353.6:p.Val103Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.373G>A
  hgvsp: ENSP00000379500.2:p.Val125Ile
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.315G>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.144G>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7981
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val125Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-18588015-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588015
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588015
    reference: chr 11
allele count: 1
allele frequency: 8.348220994106157e-6
allele num: 119786
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.258T>G
  hgvsp: ENSP00000441092.1:p.Ile86Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.306T>G
  hgvsp: ENSP00000323353.6:p.Ile102Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.372T>G
  hgvsp: ENSP00000300038.7:p.Ile124Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.306T>G
  hgvsp: ENSP00000368697.4:p.Ile102Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1458T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.372T>G
  hgvsp: ENSP00000442974.1:p.Ile124Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.143T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.372T>G
  hgvsp: ENSP00000379500.2:p.Ile124Met
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.314T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.*10T>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile124Met
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-18588033-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588033
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588033
    reference: chr 11
allele count: 11
allele frequency: 9.43768553631793e-5
allele num: 116554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-4A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.358-4A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.292-4A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.244-4A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.292-4A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.358-4A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1476A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-4A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.358-4A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.300-4A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11792
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 2.75e1
  variant carriers: 0
hgvs: c.358-4A>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-18588042-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588042
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588043
    reference: chr 11
allele count: 1
allele frequency: 8.747528823107472e-6
allele num: 114318
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.292-14dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.358-14dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-14dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1486dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.358-14dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.292-14dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.244-14dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.300-14dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-14dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.358-14dupT
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24009
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6029
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33299
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

11-18588058-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588058
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588058
    reference: chr 11
allele count: 1
allele frequency: 8.959931187728478e-6
allele num: 111608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-29A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1501A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.292-29A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.292-29A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.244-29A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.358-29A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.358-29A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-29A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.300-29A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.358-29A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-18588061-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588061
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588061
    reference: chr 11
allele count: 1
allele frequency: 8.999928000575996e-6
allele num: 111112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.292-32T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.292-32T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-32T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.358-32T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1504T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.244-32T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.300-32T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-32T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.358-32T>C
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.358-32T>C
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17595
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12763
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-18588063-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588063
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588063
    reference: chr 11
allele count: 14
allele frequency: 1.263834473793489e-4
allele num: 110774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1506T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.244-34T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.358-34T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.358-34T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-34T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.300-34T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-34T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.292-34T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.358-34T>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.292-34T>G
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17928
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10631
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS

11-18588072-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588072
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588072
    reference: chr 11
allele count: 8
allele frequency: 7.420874921153204e-5
allele num: 107804
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.292-43C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.292-43C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1515C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.358-43C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-43C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.244-43C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-43C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.358-43C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.300-43C>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.358-43C>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6920
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17368
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16111
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8931
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2825
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7272
  bin: 3.75e1
  variant carriers: 0
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: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-18588077-A-AGGTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588077
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588082
    reference: chr 11
allele count: 1
allele frequency: 9.449116507606538e-6
allele num: 105830
alternate allele: AGGTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1521_194-1520insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.358-49_358-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.244-49_244-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.292-49_292-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-49_129-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-49_194-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.292-49_292-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.358-49_358-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.300-49_300-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.358-49_358-48insAAACC
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16824
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6021
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2053
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

11-18588079-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18588079
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18588079
    reference: chr 11
allele count: 1
allele frequency: 9.58148091369002e-6
allele num: 104368
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.358-50T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.244-50T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-50T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.292-50T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.358-50T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.358-50T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-1522T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-50T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.300-50T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.292-50T>A
  variant of: http://identifiers.org/hgnc/30866
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16694
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15755
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

11-18591713-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591713
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591713
    reference: chr 11
allele count: 1
allele frequency: 1.007089912987432e-5
allele num: 99296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3684A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+48A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3684A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+48A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+48A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-5156A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+48A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+48A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.456A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+48A>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+48A>G
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16855
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8793
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-18591715-TAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591713
    reference: chr 11
allele count: 410
allele frequency: 5.227991431194532e-3
allele num: 78424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-5160_194-5159delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+44_291+45delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+44_357+45delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+44_357+45delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+44_299+45delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3688_129-3687delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+44_243+45delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+44_291+45delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.452_453delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3688_194-3687delTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+44_357+45delTT
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 1.75e1
  variant carriers: 243
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 2.25e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 16821
  bin: 1.25e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 3.75e1
  variant carriers: 19
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: TAA
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-18591715-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591716
    reference: chr 11
allele count: 21409
allele frequency: 2.729904110986432e-1
allele num: 78424
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3687dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-5159dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+45dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+45dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+45dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+45dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+45dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.453dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+45dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+45dupT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3687dupT
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 2.25e1
  variant carriers: 3970
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 549
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 1.75e1
  variant carriers: 8250
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 1524
genotype depth: GenotypeDepth
  all individuals: 16821
  bin: 1.25e1
  variant carriers: 8709
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 7.5e0
  variant carriers: 2964
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 294
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 1.25e1
  variant carriers: 837
num of homozygotes: 56
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

11-18591715-T-TAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591717
    reference: chr 11
allele count: 453
allele frequency: 5.776292971539324e-3
allele num: 78424
alternate allele: TAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+44_357+45dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+44_299+45dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3688_129-3687dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-5160_194-5159dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.452_453dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+44_291+45dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+44_291+45dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+44_357+45dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3688_194-3687dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+44_357+45dupTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+44_243+45dupTT
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16821
  bin: 1.25e1
  variant carriers: 262
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 7.5e0
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 1.75e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 2.25e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 8.75e1
  variant carriers: 20
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-18591715-T-TAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591718
    reference: chr 11
allele count: 4
allele frequency: 5.100479445067836e-5
allele num: 78424
alternate allele: TAAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-5161_194-5159dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+43_291+45dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+43_243+45dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+43_291+45dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+43_357+45dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+43_299+45dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+43_357+45dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.451_453dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3689_129-3687dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+43_357+45dupTTT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3689_194-3687dupTTT
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16821
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

11-18591715-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591714
    reference: chr 11
allele count: 17035
allele frequency: 2.172166683668265e-1
allele num: 78424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.453delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+45delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3687delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+45delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+45delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-5159delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+45delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+45delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+45delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+45delT
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3687delT
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 2.25e1
  variant carriers: 4291
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 700
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 1721
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 1.75e1
  variant carriers: 6571
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 7.5e0
  variant carriers: 886
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 16821
  bin: 1.25e1
  variant carriers: 4941
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 7.25e1
  variant carriers: 922
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: TA
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-18591715-TAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591712
    reference: chr 11
allele count: 8
allele frequency: 1.020095889013567e-4
allele num: 78424
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16821
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1909
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2196
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11867
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12024
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2178
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 9.602458229306702e-5
  allele num: 10414
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.275835672365399e-4
  allele num: 7838
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 1.70590242238144e-4
  allele num: 5862
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 596
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TAAA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-18591716-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591716
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591716
    reference: chr 11
allele count: 2
allele frequency: 1.628664495114007e-3
allele num: 1228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3687T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+45T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+45T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+45T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+45T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.453T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3687T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+45T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-5159T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+45T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+45T>A
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-18591723-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591723
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591723
    reference: chr 11
allele count: 6
allele frequency: 5.214761250847399e-5
allele num: 115058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+38T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.194-5166T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3694T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+38T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+38T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+38T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+38T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.446T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3694T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+38T>A
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+38T>A
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11929
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13508
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4768
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

11-18591730-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18591730
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 18591730
    reference: chr 11
allele count: 1
allele frequency: 9.478133944988911e-6
allele num: 105506
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000368697
  ensembl transcript: ENST00000379387
  gene symbol: UEVLD
  hgvsc: ENST00000379387.4:c.291+31C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540917
  gene symbol: UEVLD
  hgvsc: ENST00000540917.1:n.299+31C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000300038
  ensembl transcript: ENST00000300038
  gene symbol: UEVLD
  hgvsc: ENST00000300038.7:c.357+31C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000442974
  ensembl transcript: ENST00000543987
  gene symbol: UEVLD
  hgvsc: ENST00000543987.1:c.357+31C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000535340
  gene symbol: UEVLD
  hgvsc: ENST00000535340.1:n.439C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl transcript: ENST00000540666
  gene symbol: UEVLD
  hgvsc: ENST00000540666.1:n.129-3701C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000441092
  ensembl transcript: ENST00000535484
  gene symbol: UEVLD
  hgvsc: ENST00000535484.1:c.243+31C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000323353
  ensembl transcript: ENST00000320750
  gene symbol: UEVLD
  hgvsc: ENST00000320750.6:c.291+31C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379500
  ensembl transcript: ENST00000396197
  gene symbol: UEVLD
  hgvsc: ENST00000396197.3:c.357+31C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000379499
  ensembl transcript: ENST00000396196
  gene symbol: UEVLD
  hgvsc: ENST00000396196.2:c.194-3701C>G
  variant of: http://identifiers.org/hgnc/30866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151116
  ensembl protein: ENSP00000437538
  ensembl transcript: ENST00000541984
  gene symbol: UEVLD
  hgvsc: ENST00000541984.1:c.193+5164C>G
  variant of: http://identifiers.org/hgnc/30866
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15801
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3701
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

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

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

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3121
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43697
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8743
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998141152485459e-5
allele num: 66708
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.241396025206011e-4
allele num: 16504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 2.635e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

DP
type: SiteQuality
SIO_000300: 1.864607e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.318e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43721
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3112
bin: 9.75e1
variant carriers: 1

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

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

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

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 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: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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

FS
type: SiteQuality
SIO_000300: 4.441e0

DP
type: SiteQuality
SIO_000300: 1.863927e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

MQRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.2e-2

QD
type: SiteQuality
SIO_000300: 1.119e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43723
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1716
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8746
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.538e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

FS
type: SiteQuality
SIO_000300: 1.446e0

MQRankSum
type: SiteQuality
SIO_000300: -2.93e-1

DP
type: SiteQuality
SIO_000300: 1.864005e6

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

GenotypeQuality
all individuals: 1658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8746
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43723
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3113
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
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: 2.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.62e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 1.446e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

DP
type: SiteQuality
SIO_000300: 1.864005e6

QD
type: SiteQuality
SIO_000300: 1.538e1

MQ
type: SiteQuality
SIO_000300: 5.89e1

GenotypeQuality
all individuals: 43749
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3110
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.86409e6

FS
type: SiteQuality
SIO_000300: 1.0048e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.308e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

QD
type: SiteQuality
SIO_000300: 1.683e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.91e-1

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

GenotypeQuality
all individuals: 8727
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43736
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1711
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.391e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-3

DP
type: SiteQuality
SIO_000300: 1.864264e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.75e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.157999999999999e0

GenotypeQuality
all individuals: 43760
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3108
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 487
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8723
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1708
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

MQ
type: SiteQuality
SIO_000300: 5.894e1

QD
type: SiteQuality
SIO_000300: 1.422e1

FS
type: SiteQuality
SIO_000300: 7.664e0

MQRankSum
type: SiteQuality
SIO_000300: 5.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: -1.444e0

DP
type: SiteQuality
SIO_000300: 1.864097e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.34e-1

GenotypeQuality
all individuals: 1639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3110
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43764
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.68787238131847e-4
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.217e1

VQSLOD
type: SiteQuality
SIO_000300: 3.91e0

MQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.215e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.864249e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8713
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1637
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 60
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 825
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43763
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 9.75e1
variant carriers: 1

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: 11560
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.99e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.863648e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

FS
type: SiteQuality
SIO_000300: 2.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

GenotypeQuality
all individuals: 43700
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1635
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8700
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3103
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999490086685263e-5
allele num: 66678
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

FS
type: SiteQuality
SIO_000300: 1.741e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.97e-1

DP
type: SiteQuality
SIO_000300: 1.863163e6

QD
type: SiteQuality
SIO_000300: 1.421e1

GenotypeQuality
all individuals: 8524
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3088
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43320
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

FS
type: SiteQuality
SIO_000300: 2.538e0

VQSLOD
type: SiteQuality
SIO_000300: 8.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.081e0

MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

DP
type: SiteQuality
SIO_000300: 1.850214e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.412e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

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

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

GenotypeQuality
all individuals: 460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3088
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43044
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8488
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508841813024323e-5
allele num: 66276
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.896000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 1.846253e6

QD
type: SiteQuality
SIO_000300: 1.57e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.346e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: -6.021e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 813
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3088
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1513
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8484
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.525842561023444e-5
allele num: 66286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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: 16456
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.787e0

DP
type: SiteQuality
SIO_000300: 1.84579e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-2

FS
type: SiteQuality
SIO_000300: 4.749e0

QD
type: SiteQuality
SIO_000300: 1.148e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

GenotypeQuality
all individuals: 277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531159087429184e-5
allele num: 65310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

DP
type: SiteQuality
SIO_000300: 1.791237e6

FS
type: SiteQuality
SIO_000300: 6.835e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.099e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.17e-1

GenotypeQuality
all individuals: 1293
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1401
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3686
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 193
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532895947023116e-5
allele num: 65236
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.913e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

QD
type: SiteQuality
SIO_000300: 2.25e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.327e0

DP
type: SiteQuality
SIO_000300: 1.786003e6

FS
type: SiteQuality
SIO_000300: 3.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.28e0

GenotypeQuality
all individuals: 5101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 825
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7039
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3067
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.153088850603002e-5
allele num: 16252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11258
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.751856e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.264e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.89e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.295e1

GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2381
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6048
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 258
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3056
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.197318007662835e-4
allele num: 8352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63904
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16156
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.27e0

DP
type: SiteQuality
SIO_000300: 1.631283e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -7.524999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 24767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4685
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12002
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4789
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3492
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3056
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63366
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.008674601573532e-4
allele num: 9914
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11054
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.329e0

QD
type: SiteQuality
SIO_000300: 1.737e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.21e-1

FS
type: SiteQuality
SIO_000300: 2.889e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.47e-1

DP
type: SiteQuality
SIO_000300: 1.514498e6

GenotypeQuality
all individuals: 694
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8329
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5054
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13129
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2720
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61312
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.300403225806451e-5
allele num: 15872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.36e-1

FS
type: SiteQuality
SIO_000300: 1.891e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.089e1

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

DP
type: SiteQuality
SIO_000300: 1.350968e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e0

GenotypeQuality
all individuals: 3388
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7386
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11424
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7928
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2878
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7700
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59432
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.420133538777607e-5
allele num: 15576
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.076e1

VQSLOD
type: SiteQuality
SIO_000300: -1.081e0

DP
type: SiteQuality
SIO_000300: 1.321695e6

MQ
type: SiteQuality
SIO_000300: 5.896e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.111e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

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

GenotypeQuality
all individuals: 3725
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41147
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1135
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8324
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.944e1

DP
type: SiteQuality
SIO_000300: 1.803049e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.203e0

QD
type: SiteQuality
SIO_000300: 1.093e1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e-1

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 129
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3712
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2159
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.011715229798738e-5
allele num: 66580
num of homozygotes: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 1.803994e6

MQ
type: SiteQuality
SIO_000300: 6.013e1

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

VQSLOD
type: SiteQuality
SIO_000300: 3.72e0

GenotypeQuality
all individuals: 539
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8324
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41865
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 469
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21300339640951e-4
allele num: 16488
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
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: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.217e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.44e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.857e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 1.805685e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.277e0

FS
type: SiteQuality
SIO_000300: 8.534000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8329
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41905
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.806029e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

FS
type: SiteQuality
SIO_000300: 2.872e0

QD
type: SiteQuality
SIO_000300: 1.307e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2063
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8325
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42008
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1104
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2147
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 1.807088e6

VQSLOD
type: SiteQuality
SIO_000300: 2.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.715e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.779e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.096e1

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2062
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.808313e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e-2

QD
type: SiteQuality
SIO_000300: 1.524e1

GenotypeQuality
all individuals: 2063
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 42174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 9.75e1
variant carriers: 22

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
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: 16506
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.149086764838197e-4
allele num: 66686
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.45e-1

FS
type: SiteQuality
SIO_000300: 2.695e0

DP
type: SiteQuality
SIO_000300: 1.810001e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 1.122e1

GenotypeQuality
all individuals: 8325
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1102
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3682
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2141
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42230
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

QD
type: SiteQuality
SIO_000300: 1.397e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.107e0

FS
type: SiteQuality
SIO_000300: 3.843e0

DP
type: SiteQuality
SIO_000300: 1.808936e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2050
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2136
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8312
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3684
bin: 9.75e1
variant carriers: 19

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

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42227
bin: 6.25e1
variant carriers: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 18
allele frequency: 1.73176832788147e-3
allele num: 10394
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.808953e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.53e0

QD
type: SiteQuality
SIO_000300: 1.296e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

GenotypeQuality
all individuals: 42193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2122
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3616
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.352e0

FS
type: SiteQuality
SIO_000300: 6.893300000000001e1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.997e0

MQ
type: SiteQuality
SIO_000300: 5.887e1

DP
type: SiteQuality
SIO_000300: 1.805596e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.17e-1

QD
type: SiteQuality
SIO_000300: 2.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3616
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2122
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
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: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.887e1

VQSLOD
type: SiteQuality
SIO_000300: -6.352e0

DP
type: SiteQuality
SIO_000300: 1.805596e6

FS
type: SiteQuality
SIO_000300: 6.893300000000001e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.997e0

QD
type: SiteQuality
SIO_000300: 2.05e0

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

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3649
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 466
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8277
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42216
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.005e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.818e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

DP
type: SiteQuality
SIO_000300: 1.803633e6

VQSLOD
type: SiteQuality
SIO_000300: 9.350000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.57e0

QD
type: SiteQuality
SIO_000300: 2.488e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.47e-1

GenotypeQuality
all individuals: 793
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1984
bin: 7.25e1
variant carriers: 9

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 119
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 166
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 180
bin: 5.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2290
bin: 9.75e1
variant carriers: 205

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2030
bin: 7.75e1
variant carriers: 9

GenotypeQuality
all individuals: 136
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 138
bin: 3.75e1
variant carriers: 7

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 464
bin: 9.25e1
variant carriers: 12

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 8169
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1014
bin: 8.25e1
variant carriers: 6

Latino
type: Population
allele count: 5
allele frequency: 4.350095702105446e-4
allele num: 11494
num of homozygotes: 0

Other
type: Population
allele count: 10
allele frequency: 1.131221719457014e-2
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 35
allele frequency: 3.479125248508947e-3
allele num: 10060
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 149
allele frequency: 2.273975947744338e-3
allele num: 65524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 110
allele frequency: 1.795039164490862e-2
allele num: 6128
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.657661853749418e-4
allele num: 8588
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.275e0

FS
type: SiteQuality
SIO_000300: 2.53298e2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.687e0

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.952e2

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e0

QD
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.80189e6

GenotypeQuality
all individuals: 1153
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2234
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.158e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.778e0

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.008e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 1.739176e6

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2308
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8498
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 480
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1153
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

QD
type: SiteQuality
SIO_000300: 1.158e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.739176e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.008e0

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

FS
type: SiteQuality
SIO_000300: 5.778e0

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-2

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43317
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8494
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 480
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1152
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.826e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.69e-1

DP
type: SiteQuality
SIO_000300: 1.739221e6

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2230
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43331
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8499
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.419e0

MQRankSum
type: SiteQuality
SIO_000300: -1.018e0

DP
type: SiteQuality
SIO_000300: 1.739202e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.018e0

QD
type: SiteQuality
SIO_000300: 1.535e1

FS
type: SiteQuality
SIO_000300: 1.154e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.73e-1

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

GenotypeQuality
all individuals: 2091
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8493
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43334
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 539
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 481
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1147
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2299
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 9.51e0

DP
type: SiteQuality
SIO_000300: 1.739002e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2297
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8478
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1145
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.738511e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: -6.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.206e1

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

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

GenotypeQuality
all individuals: 8480
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43322
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2228
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.738366e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

VQSLOD
type: SiteQuality
SIO_000300: -1.019e0

MQRankSum
type: SiteQuality
SIO_000300: 8.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.25e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 1.1229e1

QD
type: SiteQuality
SIO_000300: 1.325e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43285
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.738051e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

FS
type: SiteQuality
SIO_000300: 7.79e-1

QD
type: SiteQuality
SIO_000300: 1.362e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

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

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

GenotypeQuality
all individuals: 1144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43285
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 538
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

DP
type: SiteQuality
SIO_000300: 1.738051e6

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.79e-1

QD
type: SiteQuality
SIO_000300: 1.362e1

GenotypeQuality
all individuals: 8464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43320
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2081
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 538
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2223
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 9.75e1
variant carriers: 2

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.395e0

VQSLOD
type: SiteQuality
SIO_000300: -7.442e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.35e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.737817e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

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

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

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43315
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.888e1

DP
type: SiteQuality
SIO_000300: 1.737833e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-1

FS
type: SiteQuality
SIO_000300: 9.805999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.783e0

QD
type: SiteQuality
SIO_000300: 1.439e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.208e0

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 537
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8462
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43332
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.948850178394747e-4
allele num: 66706
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

DP
type: SiteQuality
SIO_000300: 1.737884e6

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8430
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 141
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2073
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2212
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 1.735607e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 6.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

QD
type: SiteQuality
SIO_000300: 1.409e1

GenotypeQuality
all individuals: 470
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8420
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2271
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

DP
type: SiteQuality
SIO_000300: 1.734813e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.424e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2062
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8415
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2207
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43268
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 6.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.903e0

FS
type: SiteQuality
SIO_000300: 6.204e0

MQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.95e-1

DP
type: SiteQuality
SIO_000300: 1.734331e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.337e1

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8236
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 517
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42909
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
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: 16456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66338
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.675e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.721502e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.798e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.702e1

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

GenotypeQuality
all individuals: 1387
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1036
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 432
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42056
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 3.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52114390021296e-5
allele num: 65740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.888e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.557e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.91e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.85e-1

DP
type: SiteQuality
SIO_000300: 1.700358e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 1470
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42062
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 209
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2234
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.775008775008775e-5
allele num: 11396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.65e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.34e1

DP
type: SiteQuality
SIO_000300: 1.698093e6

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.18e0

GenotypeQuality
all individuals: 37775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7145
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 954
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 184
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5159
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.968102073365231e-4
allele num: 10032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.061254077564335e-5
allele num: 11036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63680
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.707e0

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

QD
type: SiteQuality
SIO_000300: 1.632e1

DP
type: SiteQuality
SIO_000300: 1.60694e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 908
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.604569814832643e-5
allele num: 62322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8064
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

DP
type: SiteQuality
SIO_000300: 1.515092e6

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 4230
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12552
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6447
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3740
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.15473441108545e-3
allele num: 866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.4e-2

DP
type: SiteQuality
SIO_000300: 1.301272e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-2

FS
type: SiteQuality
SIO_000300: 2.152e0

QD
type: SiteQuality
SIO_000300: 1.625e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.374e0

GenotypeQuality
all individuals: 775
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4315
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4482
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18540
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7812
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.045806316670153e-4
allele num: 9562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10446
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.027e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.071e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.656e0

DP
type: SiteQuality
SIO_000300: 1.274641e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
all individuals: 4653
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 332
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7630
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12899
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2202
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 4944
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3253
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.941116362242943e-4
allele num: 15658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.38e-1

DP
type: SiteQuality
SIO_000300: 1.250942e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

QD
type: SiteQuality
SIO_000300: 1.473e1

FS
type: SiteQuality
SIO_000300: 2.067e0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 987
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3065
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12013
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2333
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1086
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9407
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.137690094533498e-5
allele num: 58392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.252244048393391e-4
allele num: 15374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6224
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-1

DP
type: SiteQuality
SIO_000300: 1.172466e6

VQSLOD
type: SiteQuality
SIO_000300: 2.75e0

QD
type: SiteQuality
SIO_000300: 1.113e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.271e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1828
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9059
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5014
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4593
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
bin: 5.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1227
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3277
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7703
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10719
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.750087504375219e-5
allele num: 57140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6168
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

DP
type: SiteQuality
SIO_000300: 1.149025e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 4.129e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.516e0

QD
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: 3.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.575e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

GenotypeQuality
all individuals: 1269
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3314
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7706
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2849
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9961
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8994
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4976
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4964
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.777209070875098e-5
allele num: 56268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.207e0

MQ
type: SiteQuality
SIO_000300: 4.129e1

MQRankSum
type: SiteQuality
SIO_000300: -1.071e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 2.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.78e-1

DP
type: SiteQuality
SIO_000300: 1.145059e6

GenotypeQuality
all individuals: 7094
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4427
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2730
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4283
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5340
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10072
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.827752595408685e-5
allele num: 54712
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

QD
type: SiteQuality
SIO_000300: 5.83e0

MQRankSum
type: SiteQuality
SIO_000300: -1.423e0

DP
type: SiteQuality
SIO_000300: 1.257407e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e0

MQ
type: SiteQuality
SIO_000300: 6.033e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.497e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.009e0

GenotypeQuality
all individuals: 1682
bin: 8.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1882
bin: 2.75e1
variant carriers: 41

GenotypeQuality
all individuals: 2196
bin: 6.25e1
variant carriers: 36

GenotypeQuality
all individuals: 1500
bin: 9.25e1
variant carriers: 13

GenotypeQuality
all individuals: 1968
bin: 2.25e1
variant carriers: 23

GenotypeQuality
all individuals: 2044
bin: 7.25e1
variant carriers: 26

GenotypeQuality
all individuals: 12024
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 1546
bin: 1.25e1
variant carriers: 26

GenotypeQuality
all individuals: 1692
bin: 1.75e1
variant carriers: 22

GenotypeQuality
all individuals: 2178
bin: 6.75e1
variant carriers: 32

GenotypeQuality
all individuals: 1967
bin: 3.25e1
variant carriers: 43

GenotypeQuality
all individuals: 2012
bin: 7.5e0
variant carriers: 79

GenotypeQuality
all individuals: 11867
bin: 2.5e0
variant carriers: 90

GenotypeQuality
all individuals: 2381
bin: 4.25e1
variant carriers: 27

GenotypeQuality
all individuals: 1909
bin: 7.75e1
variant carriers: 22

GenotypeQuality
all individuals: 2247
bin: 5.75e1
variant carriers: 26

GenotypeQuality
all individuals: 2497
bin: 4.75e1
variant carriers: 28

GenotypeQuality
all individuals: 2365
bin: 5.25e1
variant carriers: 20

GenotypeQuality
all individuals: 1696
bin: 8.25e1
variant carriers: 26

East Asian
type: Population
allele count: 12
allele frequency: 2.047082906857728e-3
allele num: 5862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 8.190008190008191e-4
allele num: 4884
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.355704697986577e-3
allele num: 596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 257
allele frequency: 6.032863849765258e-3
allele num: 42600
num of homozygotes: 0

African
type: Population
allele count: 25
allele frequency: 4.012841091492777e-3
allele num: 6230
num of homozygotes: 0

Latino
type: Population
allele count: 28
allele frequency: 3.572339882623118e-3
allele num: 7838
num of homozygotes: 0

South Asian
type: Population
allele count: 82
allele frequency: 7.874015748031496e-3
allele num: 10414
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

DP
type: SiteQuality
SIO_000300: 1.07347e6

QD
type: SiteQuality
SIO_000300: 5.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.111e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

GenotypeQuality
all individuals: 2497
bin: 4.75e1
variant carriers: 1293

GenotypeQuality
all individuals: 2170
bin: 3.75e1
variant carriers: 1158

GenotypeQuality
all individuals: 1882
bin: 2.75e1
variant carriers: 971

GenotypeQuality
all individuals: 2381
bin: 4.25e1
variant carriers: 1196

GenotypeQuality
all individuals: 2012
bin: 7.5e0
variant carriers: 903

GenotypeQuality
all individuals: 1968
bin: 2.25e1
variant carriers: 938

GenotypeQuality
all individuals: 1696
bin: 8.25e1
variant carriers: 950

GenotypeQuality
all individuals: 1692
bin: 1.75e1
variant carriers: 969

GenotypeQuality
all individuals: 2044
bin: 7.25e1
variant carriers: 1103

GenotypeQuality
all individuals: 2196
bin: 6.25e1
variant carriers: 1149

GenotypeQuality
all individuals: 2365
bin: 5.25e1
variant carriers: 1283

GenotypeQuality
all individuals: 11867
bin: 2.5e0
variant carriers: 748

GenotypeQuality
all individuals: 1909
bin: 7.75e1
variant carriers: 1004

GenotypeQuality
all individuals: 12024
bin: 9.75e1
variant carriers: 7542

GenotypeQuality
all individuals: 1967
bin: 3.25e1
variant carriers: 1029

GenotypeQuality
all individuals: 1682
bin: 8.75e1
variant carriers: 1019

GenotypeQuality
all individuals: 1500
bin: 9.25e1
variant carriers: 833

GenotypeQuality
all individuals: 2178
bin: 6.75e1
variant carriers: 1205

GenotypeQuality
all individuals: 2247
bin: 5.75e1
variant carriers: 1138

European (Finnish)
type: Population
allele count: 1464
allele frequency: 2.997542997542997e-1
allele num: 4884
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 10259
allele frequency: 2.408215962441315e-1
allele num: 42600
num of homozygotes: 19

Other
type: Population
allele count: 172
allele frequency: 2.885906040268457e-1
allele num: 596
num of homozygotes: 2

South Asian
type: Population
allele count: 3286
allele frequency: 3.155367774150182e-1
allele num: 10414
num of homozygotes: 12

African
type: Population
allele count: 1416
allele frequency: 2.272873194221509e-1
allele num: 6230
num of homozygotes: 6

East Asian
type: Population
allele count: 2099
allele frequency: 3.580689184578642e-1
allele num: 5862
num of homozygotes: 9

Latino
type: Population
allele count: 2713
allele frequency: 3.461342179127329e-1
allele num: 7838
num of homozygotes: 6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.07347e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.111e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

QD
type: SiteQuality
SIO_000300: 5.03e0

GenotypeQuality
all individuals: 2247
bin: 5.75e1
variant carriers: 24

GenotypeQuality
all individuals: 2365
bin: 5.25e1
variant carriers: 29

GenotypeQuality
all individuals: 2012
bin: 7.5e0
variant carriers: 59

GenotypeQuality
all individuals: 2381
bin: 4.25e1
variant carriers: 34

GenotypeQuality
all individuals: 11867
bin: 2.5e0
variant carriers: 43

GenotypeQuality
all individuals: 2196
bin: 6.25e1
variant carriers: 26

GenotypeQuality
all individuals: 1967
bin: 3.25e1
variant carriers: 28

GenotypeQuality
all individuals: 1882
bin: 2.75e1
variant carriers: 46

GenotypeQuality
all individuals: 1546
bin: 1.25e1
variant carriers: 51

GenotypeQuality
all individuals: 1696
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1692
bin: 1.75e1
variant carriers: 35

GenotypeQuality
all individuals: 2170
bin: 3.75e1
variant carriers: 29

GenotypeQuality
all individuals: 2044
bin: 7.25e1
variant carriers: 25

GenotypeQuality
all individuals: 1909
bin: 7.75e1
variant carriers: 20

GenotypeQuality
all individuals: 1968
bin: 2.25e1
variant carriers: 46

GenotypeQuality
all individuals: 12024
bin: 9.75e1
variant carriers: 141

GenotypeQuality
all individuals: 1500
bin: 9.25e1
variant carriers: 18

GenotypeQuality
all individuals: 2497
bin: 4.75e1
variant carriers: 34

GenotypeQuality
all individuals: 2178
bin: 6.75e1
variant carriers: 21

South Asian
type: Population
allele count: 45
allele frequency: 4.321106203188016e-3
allele num: 10414
num of homozygotes: 0

African
type: Population
allele count: 51
allele frequency: 8.186195826645265e-3
allele num: 6230
num of homozygotes: 0

East Asian
type: Population
allele count: 19
allele frequency: 3.241214602524735e-3
allele num: 5862
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.677852348993289e-3
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 47
allele frequency: 5.996427660117377e-3
allele num: 7838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 1.023751023751024e-3
allele num: 4884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 285
allele frequency: 6.690140845070422e-3
allele num: 42600
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.111e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

DP
type: SiteQuality
SIO_000300: 1.07347e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 5.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

GenotypeQuality
all individuals: 1967
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 11867
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2497
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1909
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 3.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1546
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1882
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2247
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1500
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12024
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 1.275835672365399e-4
allele num: 7838
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.694835680751174e-5
allele num: 42600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4884
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.602458229306702e-5
allele num: 10414
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.111e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

QD
type: SiteQuality
SIO_000300: 5.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

DP
type: SiteQuality
SIO_000300: 1.07347e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeQuality
all individuals: 11867
bin: 2.5e0
variant carriers: 544

GenotypeQuality
all individuals: 2381
bin: 4.25e1
variant carriers: 1140

GenotypeQuality
all individuals: 12024
bin: 9.75e1
variant carriers: 4335

GenotypeQuality
all individuals: 1692
bin: 1.75e1
variant carriers: 589

GenotypeQuality
all individuals: 2170
bin: 3.75e1
variant carriers: 962

GenotypeQuality
all individuals: 2497
bin: 4.75e1
variant carriers: 1176

GenotypeQuality
all individuals: 1967
bin: 3.25e1
variant carriers: 819

GenotypeQuality
all individuals: 1882
bin: 2.75e1
variant carriers: 844

GenotypeQuality
all individuals: 2012
bin: 7.5e0
variant carriers: 605

GenotypeQuality
all individuals: 1696
bin: 8.25e1
variant carriers: 713

GenotypeQuality
all individuals: 1546
bin: 1.25e1
variant carriers: 481

GenotypeQuality
all individuals: 1968
bin: 2.25e1
variant carriers: 686

GenotypeQuality
all individuals: 2365
bin: 5.25e1
variant carriers: 1085

GenotypeQuality
all individuals: 1682
bin: 8.75e1
variant carriers: 631

GenotypeQuality
all individuals: 2196
bin: 6.25e1
variant carriers: 984

GenotypeQuality
all individuals: 1909
bin: 7.75e1
variant carriers: 889

GenotypeQuality
all individuals: 2247
bin: 5.75e1
variant carriers: 1102

GenotypeQuality
all individuals: 2178
bin: 6.75e1
variant carriers: 942

GenotypeQuality
all individuals: 1500
bin: 9.25e1
variant carriers: 635

Other
type: Population
allele count: 125
allele frequency: 2.097315436241611e-1
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 1226
allele frequency: 1.564174534319979e-1
allele num: 7838
num of homozygotes: 0

African
type: Population
allele count: 1562
allele frequency: 2.507223113964687e-1
allele num: 6230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 899
allele frequency: 1.840704340704341e-1
allele num: 4884
num of homozygotes: 0

South Asian
type: Population
allele count: 1963
allele frequency: 1.884962550412906e-1
allele num: 10414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10416
allele frequency: 2.445070422535211e-1
allele num: 42600
num of homozygotes: 0

East Asian
type: Population
allele count: 844
allele frequency: 1.439781644489935e-1
allele num: 5862
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.111e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

DP
type: SiteQuality
SIO_000300: 1.07347e6

QD
type: SiteQuality
SIO_000300: 5.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.173708920187793e-4
allele num: 42600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4884
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.111e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 5.03e0

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

DP
type: SiteQuality
SIO_000300: 1.07347e6

GenotypeQuality
all individuals: 529
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23247
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 217
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.0e-3
allele num: 200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.291989664082687e-3
allele num: 774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: 4.18e-1

FS
type: SiteQuality
SIO_000300: 4.191e0

VQSLOD
type: SiteQuality
SIO_000300: 4.36e0

QD
type: SiteQuality
SIO_000300: 3.19e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 6.46756e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.922e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

GenotypeQuality
all individuals: 7448
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2614
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5441
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4391
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21894
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1199
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3908
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.910891715714196e-5
allele num: 63204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.533742331288344e-4
allele num: 6520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9462
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15824
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.459e0

MQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.031e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

DP
type: SiteQuality
SIO_000300: 1.407806e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 1.917e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

QD
type: SiteQuality
SIO_000300: 1.486e1