4-52757895-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757895
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757895
    reference: chr 4
allele count: 128
allele frequency: 1.326342403581125e-3
allele num: 96506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5091T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-31T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-31T>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7598
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

4-52757902-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757902
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757902
    reference: chr 4
allele count: 1
allele frequency: 9.284533823556719e-6
allele num: 107706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5098T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-24T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-24T>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

4-52757902-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757902
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757901
    reference: chr 4
allele count: 1
allele frequency: 9.284533823556719e-6
allele num: 107706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5100delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-22delA
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-22delA
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: TA
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

4-52757904-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757904
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757904
    reference: chr 4
allele count: 1
allele frequency: 9.041591320072333e-6
allele num: 110600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5100A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-22A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-22A>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

4-52757905-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757905
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757905
    reference: chr 4
allele count: 10
allele frequency: 8.927774305865548e-5
allele num: 112010
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5101T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-21T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-21T>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

4-52757909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757909
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757909
    reference: chr 4
allele count: 1
allele frequency: 8.658008658008657e-6
allele num: 115500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5105G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-17G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-17G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-52757911-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757911
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757912
    reference: chr 4
allele count: 48
allele frequency: 4.297917300907935e-4
allele num: 111682
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-6dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5116dupT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-6dupT
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8904
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

4-52757911-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757911
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757911
    reference: chr 4
allele count: 1
allele frequency: 8.953994376891531e-6
allele num: 111682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5107A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-15A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-15A>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21589
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

4-52757911-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757911
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757910
    reference: chr 4
allele count: 127
allele frequency: 1.137157285865224e-3
allele num: 111682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5116delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-6delT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-6delT
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 3.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8904
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 2.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 21589
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: AT
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-52757920-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757920
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757920
    reference: chr 4
allele count: 1
allele frequency: 8.373245805003851e-6
allele num: 119428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*45-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*840-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.547-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*503-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.471-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.72-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.415-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.235-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.415-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*234-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.230-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*589-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.547-6T>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5116T>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.415-6T>A
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-52757928-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757928
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757928
    reference: chr 4
allele count: 17
allele frequency: 1.412804999667575e-4
allele num: 120328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*236A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.549A>C
  hgvsp: ENST00000505403.1:c.549A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.473A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.237A>C
  hgvsp: ENST00000381437.4:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*47A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.74A>C
  hgvsp: ENST00000505634.1:c.74A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.549A>C
  hgvsp: ENST00000451288.2:c.549A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.417A>C
  hgvsp: ENST00000334635.5:c.417A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*591A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*505A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*842A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.417A>C
  hgvsp: ENST00000381441.3:c.417A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5124A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.232A>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.417A>C
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

4-52757938-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757938
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757938
    reference: chr 4
allele count: 1
allele frequency: 8.277460475126231e-6
allele num: 120810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*515G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.483G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.84G>A
  hgvsp: ENSP00000422711.1:p.Val29Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*57G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*601G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*246G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.559G>A
  hgvsp: ENSP00000426982.1:p.Val187Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.427G>A
  hgvsp: ENSP00000334625.5:p.Val143Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*852G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.427G>A
  hgvsp: ENSP00000370850.3:p.Val143Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.247G>A
  hgvsp: ENSP00000370846.4:p.Val83Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.559G>A
  hgvsp: ENSP00000389900.2:p.Val187Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5134G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.242G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13357
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val143Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

4-52757947-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757947
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757947
    reference: chr 4
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.436T>C
  hgvsp: ENSP00000370850.3:p.Trp146Arg
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*66T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.93T>C
  hgvsp: ENSP00000422711.1:p.Trp32Arg
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.568T>C
  hgvsp: ENSP00000426982.1:p.Trp190Arg
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5143T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.492T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.568T>C
  hgvsp: ENSP00000389900.2:p.Trp190Arg
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.256T>C
  hgvsp: ENSP00000370846.4:p.Trp86Arg
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*255T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.436T>C
  hgvsp: ENSP00000334625.5:p.Trp146Arg
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*861T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*524T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.251T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*610T>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp146Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

4-52757953-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757953
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757953
    reference: chr 4
allele count: 3
allele frequency: 2.477291494632535e-5
allele num: 121100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.574T>C
  hgvsp: ENST00000451288.2:c.574T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*261T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.99T>C
  hgvsp: ENST00000505634.1:c.99T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.257T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.442T>C
  hgvsp: ENST00000381441.3:c.442T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*530T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5149T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*616T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.442T>C
  hgvsp: ENST00000334635.5:c.442T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*72T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.498T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.262T>C
  hgvsp: ENST00000381437.4:c.262T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.574T>C
  hgvsp: ENST00000505403.1:c.574T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*867T>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9501
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu148Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD

4-52757961-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757961
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757961
    reference: chr 4
allele count: 2
allele frequency: 1.650110557407346e-5
allele num: 121204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.582A>G
  hgvsp: ENST00000505403.1:c.582A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*538A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*80A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.265A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*875A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.450A>G
  hgvsp: ENST00000381441.3:c.450A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.450A>G
  hgvsp: ENST00000334635.5:c.450A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*269A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.270A>G
  hgvsp: ENST00000381437.4:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.582A>G
  hgvsp: ENST00000451288.2:c.582A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*624A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5157A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.506A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.107A>G
  hgvsp: ENST00000505634.1:c.107A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala150Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

4-52757965-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757965
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757965
    reference: chr 4
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*628A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.454A>G
  hgvsp: ENSP00000370850.3:p.Asn152Asp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.586A>G
  hgvsp: ENSP00000426982.1:p.Asn196Asp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.454A>G
  hgvsp: ENSP00000334625.5:p.Asn152Asp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.111A>G
  hgvsp: ENSP00000422711.1:p.Asn38Asp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*273A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.274A>G
  hgvsp: ENSP00000370846.4:p.Asn92Asp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*542A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5161A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.586A>G
  hgvsp: ENSP00000389900.2:p.Asn196Asp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.269A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.510A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*879A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*84A>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9506
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn152Asp
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

4-52757983-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757983
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757983
    reference: chr 4
allele count: 2
allele frequency: 1.648886177387175e-5
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*897C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.292C>G
  hgvsp: ENSP00000370846.4:p.Leu98Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.129C>G
  hgvsp: ENSP00000422711.1:p.Leu44Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5179C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.11C>G
  hgvsp: ENSP00000426048.1:p.Ser4Cys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.472C>G
  hgvsp: ENSP00000334625.5:p.Leu158Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.472C>G
  hgvsp: ENSP00000370850.3:p.Leu158Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.604C>G
  hgvsp: ENSP00000426982.1:p.Leu202Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*102C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*646C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.287C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.604C>G
  hgvsp: ENSP00000389900.2:p.Leu202Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*560C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.528C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*291C>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu158Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-52757986-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757986
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757986
    reference: chr 4
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*649C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.290C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*900C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.14C>A
  hgvsp: ENSP00000426048.1:p.Thr5Lys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.475C>A
  hgvsp: ENSP00000370850.3:p.Gln159Lys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.132C>A
  hgvsp: ENSP00000422711.1:p.Gln45Lys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.295C>A
  hgvsp: ENSP00000370846.4:p.Gln99Lys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425792
  ensembl transcript: ENST00000502930
  gene symbol: DCUN1D4
  hgvsc: ENST00000502930.1:c.*294C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.607C>A
  hgvsp: ENSP00000389900.2:p.Gln203Lys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.607C>A
  hgvsp: ENSP00000426982.1:p.Gln203Lys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*105C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.475C>A
  hgvsp: ENSP00000334625.5:p.Gln159Lys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.531C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5182C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*563C>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln159Lys
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-52757999-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52757999
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52757999
    reference: chr 4
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.488A>C
  hgvsp: ENSP00000334625.5:p.Lys163Thr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.620A>C
  hgvsp: ENSP00000426982.1:p.Lys207Thr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*576A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*118A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.620A>C
  hgvsp: ENSP00000389900.2:p.Lys207Thr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.303A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.27A>C
  hgvsp: ENSP00000426048.1:p.Lys9Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.145A>C
  hgvsp: ENSP00000422711.1:p.Lys49Thr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*662A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*913A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.488A>C
  hgvsp: ENSP00000370850.3:p.Lys163Thr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5195A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.308A>C
  hgvsp: ENSP00000370846.4:p.Lys103Thr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.544A>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys163Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/4-52758008-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758008
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758008
    reference: chr 4
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5204C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.36C>A
  hgvsp: ENSP00000426048.1:p.Asp12Glu
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000504923
  gene symbol: DCUN1D4
  hgvsc: ENST00000504923.1:n.553C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.629C>A
  hgvsp: ENSP00000389900.2:p.Thr210Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.317C>A
  hgvsp: ENSP00000370846.4:p.Thr106Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*585C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.497C>A
  hgvsp: ENSP00000370850.3:p.Thr166Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*922C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.154C>A
  hgvsp: ENSP00000422711.1:p.Thr52Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426982
  ensembl transcript: ENST00000505403
  gene symbol: DCUN1D4
  hgvsc: ENST00000505403.1:c.629C>A
  hgvsp: ENSP00000426982.1:p.Thr210Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.497C>A
  hgvsp: ENSP00000334625.5:p.Thr166Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000421699
  ensembl transcript: ENST00000509068
  gene symbol: DCUN1D4
  hgvsc: ENST00000509068.1:c.*127C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.312C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*671C>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9526
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr166Asn
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

4-52758034-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758034
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758034
    reference: chr 4
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5230A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+17A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+17A>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

4-52758038-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758038
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758038
    reference: chr 4
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5234G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+21G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+21G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13138
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

4-52758038-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758038
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758038
    reference: chr 4
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5234G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+21G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+21G>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-52758040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758040
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758040
    reference: chr 4
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5236G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+23G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+23G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

4-52758046-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758046
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758046
    reference: chr 4
allele count: 2
allele frequency: 1.652127940787734e-5
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5242C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+29C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+29C>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

4-52758047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758047
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758047
    reference: chr 4
allele count: 2
allele frequency: 1.65188231990353e-5
allele num: 121074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5243C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+30C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+30C>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22490
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

4-52758049-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758049
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758049
    reference: chr 4
allele count: 2
allele frequency: 1.652100645971353e-5
allele num: 121058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5245T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+32T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+32T>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12817
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

4-52758064-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758064
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758064
    reference: chr 4
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5260G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+47G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+47G>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22311
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

4-52758068-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52758068
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52758068
    reference: chr 4
allele count: 3
allele frequency: 2.489750526997195e-5
allele num: 120494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.638+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.120+5264C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*931+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*680+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.326+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.506+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*594+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.163+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.321+51C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.506+51C>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-52765388-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765388
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765388
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 58154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.507-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*932-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7371T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*681-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.322-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.639-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.327-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.164-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*595-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.121-48T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.507-48T>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22501
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

4-52765421-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765421
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765421
    reference: chr 4
allele count: 4
allele frequency: 5.244250989852374e-5
allele num: 76274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*932-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.507-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.322-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.327-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*681-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.121-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*595-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7404A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.639-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.164-15A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.507-15A>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24475
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

4-52765423-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765423
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765423
    reference: chr 4
allele count: 2
allele frequency: 2.555388035673217e-5
allele num: 78266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7406T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.327-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*595-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.507-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*681-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*932-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.322-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.639-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.121-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.164-13T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.507-13T>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20144
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

4-52765426-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765426
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765426
    reference: chr 4
allele count: 1
allele frequency: 1.230496628439238e-5
allele num: 81268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7409G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.507-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.507-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.121-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.322-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*681-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.327-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*932-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.164-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.639-10G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*595-10G>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27738
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

4-52765447-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765447
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765447
    reference: chr 4
allele count: 2
allele frequency: 2.078785988982434e-5
allele num: 96210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.333C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.518C>T
  hgvsp: ENSP00000334625.5:p.Thr173Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*692C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.338C>T
  hgvsp: ENSP00000370846.4:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.175C>T
  hgvsp: ENSP00000422711.1:p.Thr59Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*943C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.132C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.518C>T
  hgvsp: ENSP00000370850.3:p.Thr173Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*606C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.650C>T
  hgvsp: ENSP00000389900.2:p.Thr217Ile
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7430C>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35219
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr173Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

4-52765454-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765454
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765454
    reference: chr 4
allele count: 1
allele frequency: 1.015537727226566e-5
allele num: 98470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.139A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.345A>T
  hgvsp: ENSP00000370846.4:p.Lys115Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.340A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.657A>T
  hgvsp: ENSP00000389900.2:p.Lys219Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.525A>T
  hgvsp: ENSP00000370850.3:p.Lys175Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*699A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.525A>T
  hgvsp: ENSP00000334625.5:p.Lys175Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7437A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.182A>T
  hgvsp: ENSP00000422711.1:p.Lys61Asn
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*950A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*613A>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys175Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

4-52765462-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765462
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765462
    reference: chr 4
allele count: 1
allele frequency: 9.959167413604222e-6
allele num: 100410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.665A>G
  hgvsp: ENSP00000389900.2:p.Asn222Ser
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7445A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.190A>G
  hgvsp: ENSP00000422711.1:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*958A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.353A>G
  hgvsp: ENSP00000370846.4:p.Asn118Ser
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.533A>G
  hgvsp: ENSP00000334625.5:p.Asn178Ser
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.533A>G
  hgvsp: ENSP00000370850.3:p.Asn178Ser
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.147A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*621A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*707A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.348A>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn178Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/4-52765483-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765483
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765483
    reference: chr 4
allele count: 1
allele frequency: 9.851634386144662e-6
allele num: 101506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.211C>A
  hgvsp: ENSP00000422711.1:p.Ser71Ter
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.554C>A
  hgvsp: ENSP00000370850.3:p.Ser185Ter
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*979C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.374C>A
  hgvsp: ENSP00000370846.4:p.Ser125Ter
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.686C>A
  hgvsp: ENSP00000389900.2:p.Ser229Ter
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.554C>A
  hgvsp: ENSP00000334625.5:p.Ser185Ter
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.369C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*728C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*642C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.168C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7466C>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser185Ter
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-52765498-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765498
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765498
    reference: chr 4
allele count: 1
allele frequency: 9.948664889171872e-6
allele num: 100516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*994C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.569C>A
  hgvsp: ENSP00000370850.3:p.Ser190Tyr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.226C>A
  hgvsp: ENSP00000422711.1:p.Ser76Tyr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.384C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.701C>A
  hgvsp: ENSP00000389900.2:p.Ser234Tyr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*657C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.389C>A
  hgvsp: ENSP00000370846.4:p.Ser130Tyr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*743C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.183C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.569C>A
  hgvsp: ENSP00000334625.5:p.Ser190Tyr
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7481C>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser190Tyr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-52765500-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765500
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765500
    reference: chr 4
allele count: 1
allele frequency: 9.992006394884094e-6
allele num: 100080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*996A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*745A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.703A>C
  hgvsp: ENSP00000389900.2:p.Thr235Pro
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*659A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.391A>C
  hgvsp: ENSP00000370846.4:p.Thr131Pro
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.228A>C
  hgvsp: ENSP00000422711.1:p.Thr77Pro
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7483A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.571A>C
  hgvsp: ENSP00000334625.5:p.Thr191Pro
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.571A>C
  hgvsp: ENSP00000370850.3:p.Thr191Pro
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.386A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.185A>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr191Pro
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

4-52765500-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765500
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765500
    reference: chr 4
allele count: 9
allele frequency: 8.992805755395684e-5
allele num: 100080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.571A>G
  hgvsp: ENSP00000370850.3:p.Thr191Ala
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.703A>G
  hgvsp: ENSP00000389900.2:p.Thr235Ala
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*996A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.391A>G
  hgvsp: ENSP00000370846.4:p.Thr131Ala
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*659A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7483A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*745A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.571A>G
  hgvsp: ENSP00000334625.5:p.Thr191Ala
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.228A>G
  hgvsp: ENSP00000422711.1:p.Thr77Ala
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.386A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.185A>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr191Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/4-52765503-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765503
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765503
    reference: chr 4
allele count: 1
allele frequency: 1.003492152691366e-5
allele num: 99652
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7486A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*999A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*662A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.706A>C
  hgvsp: ENSP00000389900.2:p.Asn236His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.394A>C
  hgvsp: ENSP00000370846.4:p.Asn132His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.1A>C
  hgvsp: ENSP00000423794.1:p.Asn1?
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.231A>C
  hgvsp: ENSP00000422711.1:p.Asn78His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.574A>C
  hgvsp: ENSP00000334625.5:p.Asn192His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.188A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.574A>C
  hgvsp: ENSP00000370850.3:p.Asn192His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.389A>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*748A>C
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn1?
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

4-52765512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765512
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765512
    reference: chr 4
allele count: 1
allele frequency: 1.011326860841424e-5
allele num: 98880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.197C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.583C>T
  hgvsp: ENSP00000370850.3:p.Leu195Phe
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.403C>T
  hgvsp: ENSP00000370846.4:p.Leu135Phe
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*757C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.715C>T
  hgvsp: ENSP00000389900.2:p.Leu239Phe
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.240C>T
  hgvsp: ENSP00000422711.1:p.Leu81Phe
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.583C>T
  hgvsp: ENSP00000334625.5:p.Leu195Phe
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1008C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.10C>T
  hgvsp: ENSP00000423794.1:p.Leu4Phe
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7495C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.398C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*671C>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu195Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

4-52765520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765520
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765520
    reference: chr 4
allele count: 2
allele frequency: 2.048592616872209e-5
allele num: 97628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.406C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*679C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.723C>T
  hgvsp: ENST00000451288.2:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.411C>T
  hgvsp: ENST00000381437.4:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.591C>T
  hgvsp: ENST00000334635.5:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.205C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.591C>T
  hgvsp: ENST00000381441.3:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1016C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.248C>T
  hgvsp: ENST00000505634.1:c.248C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.18C>T
  hgvsp: ENST00000512199.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7503C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*765C>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr197Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

4-52765526-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765526
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765526
    reference: chr 4
allele count: 14
allele frequency: 1.453729855457717e-4
allele num: 96304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.412T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*771T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.729T>C
  hgvsp: ENST00000451288.2:c.729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7509T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.597T>C
  hgvsp: ENST00000334635.5:c.597T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*685T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.417T>C
  hgvsp: ENST00000381437.4:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.254T>C
  hgvsp: ENST00000505634.1:c.254T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.24T>C
  hgvsp: ENST00000512199.1:c.24T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1022T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.597T>C
  hgvsp: ENST00000381441.3:c.597T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.211T>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8132
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27505
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr199Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-52765528-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765528
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765528
    reference: chr 4
allele count: 1
allele frequency: 1.041796891278076e-5
allele num: 95988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.26C>T
  hgvsp: ENSP00000423794.1:p.Ala9Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1024C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.599C>T
  hgvsp: ENSP00000370850.3:p.Ala200Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*687C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*773C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.599C>T
  hgvsp: ENSP00000334625.5:p.Ala200Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.419C>T
  hgvsp: ENSP00000370846.4:p.Ala140Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7511C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.213C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.731C>T
  hgvsp: ENSP00000389900.2:p.Ala244Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.256C>T
  hgvsp: ENSP00000422711.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.414C>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala200Val
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

4-52765529-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765529
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765529
    reference: chr 4
allele count: 8
allele frequency: 8.37977123224536e-5
allele num: 95468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.732G>A
  hgvsp: ENST00000451288.2:c.732G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.600G>A
  hgvsp: ENST00000334635.5:c.600G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*774G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.257G>A
  hgvsp: ENST00000505634.1:c.257G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7512G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.415G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.27G>A
  hgvsp: ENST00000512199.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1025G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.420G>A
  hgvsp: ENST00000381437.4:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*688G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.600G>A
  hgvsp: ENST00000381441.3:c.600G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.214G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala200Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

4-52765533-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765533
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765533
    reference: chr 4
allele count: 1
allele frequency: 1.059434262104037e-5
allele num: 94390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7516G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.604G>C
  hgvsp: ENSP00000334625.5:p.Asp202His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.604G>C
  hgvsp: ENSP00000370850.3:p.Asp202His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.736G>C
  hgvsp: ENSP00000389900.2:p.Asp246His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.31G>C
  hgvsp: ENSP00000423794.1:p.Asp11His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.424G>C
  hgvsp: ENSP00000370846.4:p.Asp142His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.261G>C
  hgvsp: ENSP00000422711.1:p.Asp88His
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*778G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*692G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.218G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.419G>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1029G>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp202His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

4-52765541-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765541
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765541
    reference: chr 4
allele count: 1
allele frequency: 1.082204233582962e-5
allele num: 92404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.39A>T
  hgvsp: ENST00000512199.1:c.39A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.744A>T
  hgvsp: ENST00000451288.2:c.744A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7524A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.427A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*786A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*700A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1037A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.612A>T
  hgvsp: ENST00000381441.3:c.612A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.226A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.612A>T
  hgvsp: ENST00000334635.5:c.612A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.269A>T
  hgvsp: ENST00000505634.1:c.269A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.432A>T
  hgvsp: ENST00000381437.4:c.432A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21970
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala204Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

4-52765542-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765542
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765542
    reference: chr 4
allele count: 1
allele frequency: 1.091440920302984e-5
allele num: 91622
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*787C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.613C>T
  hgvsp: ENSP00000370850.3:p.Arg205Trp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.613C>T
  hgvsp: ENSP00000334625.5:p.Arg205Trp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.745C>T
  hgvsp: ENSP00000389900.2:p.Arg249Trp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7525C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.433C>T
  hgvsp: ENSP00000370846.4:p.Arg145Trp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1038C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.270C>T
  hgvsp: ENSP00000422711.1:p.Arg91Trp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.227C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*701C>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.40C>T
  hgvsp: ENSP00000423794.1:p.Arg14Trp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.428C>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg205Trp
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

4-52765553-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765553
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765553
    reference: chr 4
allele count: 1
allele frequency: 1.13394112577675e-5
allele num: 88188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*789+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.615+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.229+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.272+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.747+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*703+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.435+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.430+9T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7536T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.42+9T>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

4-52765557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765557
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765557
    reference: chr 4
allele count: 4
allele frequency: 4.61829769546945e-5
allele num: 86612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.430+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.435+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.615+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7540G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*789+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.747+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.229+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.42+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*703+13G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.272+13G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17288
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14653
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

4-52765568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765568
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765568
    reference: chr 4
allele count: 1
allele frequency: 1.212179984484096e-5
allele num: 82496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.430+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.747+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.435+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.615+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*789+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7551G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*703+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.229+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.272+24G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.42+24G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

4-52765574-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765574
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765574
    reference: chr 4
allele count: 1
allele frequency: 1.315754848556617e-5
allele num: 76002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.430+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*703+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.229+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.435+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*789+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.747+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.42+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7557T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.615+30T>C
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.272+30T>C
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

4-52765577-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52765577
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52765577
    reference: chr 4
allele count: 14
allele frequency: 1.850383293682263e-4
allele num: 75660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.430+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.615+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.747+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.45+7560C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.272+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.435+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*703+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*789+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.229+33C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.42+33C>G
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18334
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16662
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

4-52771305-AGTTGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52771305
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52771300
    reference: chr 4
allele count: 1
allele frequency: 9.335324869305452e-5
allele num: 10712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-5927_46-5923delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*790-3777_*790-3773delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.229+5765_229+5769delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.430+5765_430+5769delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*703+5765_*703+5769delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.273-3777_273-3773delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.747+5765_747+5769delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.435+5765_435+5769delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.615+5765_615+5769delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+5765_615+5769delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.43-46_43-42delGTGTT
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+5765_*1040+5769delGTGTT
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: AGTTGT
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

4-52771314-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52771314
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52771314
    reference: chr 4
allele count: 1
allele frequency: 9.333582228859437e-5
allele num: 10714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*790-3772A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.615+5770A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.435+5770A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.430+5770A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+5770A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*703+5770A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.747+5770A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-5922A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.273-3772A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+5770A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.43-41A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.229+5770A>T
  variant of: http://identifiers.org/hgnc/28998
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

4-52771373-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52771373
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52771373
    reference: chr 4
allele count: 1
allele frequency: 9.300595238095238e-5
allele num: 10752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+5829A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-5863A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*703+5829A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.430+5829A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.747+5829A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*790-3713A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.61A>G
  hgvsp: ENSP00000423794.1:p.Ser21Gly
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.615+5829A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+5829A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.435+5829A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.229+5829A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.273-3713A>G
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser21Gly
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ

4-52771398-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52771398
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52771398
    reference: chr 4
allele count: 3
allele frequency: 2.789140944589066e-4
allele num: 10756
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-5838C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*20C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*790-3688C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-5838C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-5838C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-5838C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.273-3688C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+5854C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-5838C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+5854C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-5838C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-5838C>G
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

4-52771407-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52771407
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52771407
    reference: chr 4
allele count: 1
allele frequency: 9.298865538404315e-5
allele num: 10754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*29G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-5829G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.615+5863G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-5829G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1040+5863G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-5829G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*790-3679G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-5829G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-5829G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-5829G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.273-3679G>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-5829G>T
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

4-52775096-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52775096
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52775096
    reference: chr 4
allele count: 1
allele frequency: 9.27299703264095e-5
allele num: 10784
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-2140G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-2140G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-2140G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.616-4360G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*800G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1041-4360G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.283G>A
  hgvsp: ENSP00000422711.1:p.Gly95Asp
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-2140G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-2140G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-2140G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-2140G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*109-2140G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly95Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-52775105-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52775105
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52775105
    reference: chr 4
allele count: 1
allele frequency: 9.27299703264095e-5
allele num: 10784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-2131A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-2131A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1041-4351A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-2131A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.292A>T
  hgvsp: ENSP00000422711.1:p.Asp98Val
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*809A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-2131A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-2131A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-2131A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.616-4351A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*109-2131A>T
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-2131A>T
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp98Val
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

4-52775107-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52775107
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52775107
    reference: chr 4
allele count: 1
allele frequency: 9.271277582050807e-5
allele num: 10786
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-2129T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*811T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*109-2129T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-2129T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-2129T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-2129T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.616-4349T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1041-4349T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.294T>G
  hgvsp: ENSP00000422711.1:p.Cys99Gly
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-2129T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-2129T>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-2129T>G
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys99Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/4-52775109-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52775109
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52775109
    reference: chr 4
allele count: 4
allele frequency: 3.707823507601038e-4
allele num: 10788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-2127C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-2127C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-2127C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.296C>A
  hgvsp: ENSP00000422711.1:p.Cys99Ter
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*813C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.616-4347C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-2127C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1041-4347C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-2127C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-2127C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-2127C>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*109-2127C>A
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys99Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

4-52775110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52775110
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52775110
    reference: chr 4
allele count: 1
allele frequency: 9.271277582050807e-5
allele num: 10786
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-2126G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-2126G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.297G>A
  hgvsp: ENSP00000422711.1:p.Glu100Lys
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1041-4346G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-2126G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.616-4346G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-2126G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-2126G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*109-2126G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-2126G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*814G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-2126G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu100Lys
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-52775144-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52775144
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52775144
    reference: chr 4
allele count: 1
allele frequency: 9.27299703264095e-5
allele num: 10784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-2092A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.616-4312A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*845+3A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*109-2092A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-2092A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-2092A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-2092A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-2092A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1041-4312A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.328+3A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-2092A>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-2092A>G
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.328+3A>G
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

4-52777200-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52777200
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52777200
    reference: chr 4
allele count: 1
allele frequency: 8.258456659619451e-6
allele num: 121088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.329-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000508257
  gene symbol: DCUN1D4
  hgvsc: ENST00000508257.1:n.54-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1041-2256G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.616-2256G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*109-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510518
  gene symbol: DCUN1D4
  hgvsc: ENST00000510518.1:n.282G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-36G>A
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*846-36G>A
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18939
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

4-52777204-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 52777204
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 52777204
    reference: chr 4
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000424476
  ensembl transcript: ENST00000477560
  gene symbol: DCUN1D4
  hgvsc: ENST00000477560.1:c.*846-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423808
  ensembl transcript: ENST00000507741
  gene symbol: DCUN1D4
  hgvsc: ENST00000507741.1:c.*704-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000389900
  ensembl transcript: ENST00000451288
  gene symbol: DCUN1D4
  hgvsc: ENST00000451288.2:c.748-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510587
  gene symbol: DCUN1D4
  hgvsc: ENST00000510587.1:n.431-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370846
  ensembl transcript: ENST00000381437
  gene symbol: DCUN1D4
  hgvsc: ENST00000381437.4:c.436-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000508257
  gene symbol: DCUN1D4
  hgvsc: ENST00000508257.1:n.54-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000334625
  ensembl transcript: ENST00000334635
  gene symbol: DCUN1D4
  hgvsc: ENST00000334635.5:c.616-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000510518
  gene symbol: DCUN1D4
  hgvsc: ENST00000510518.1:n.286C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000426048
  ensembl transcript: ENST00000510808
  gene symbol: DCUN1D4
  hgvsc: ENST00000510808.1:c.46-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000370850
  ensembl transcript: ENST00000381441
  gene symbol: DCUN1D4
  hgvsc: ENST00000381441.3:c.616-2252C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000422711
  ensembl transcript: ENST00000505634
  gene symbol: DCUN1D4
  hgvsc: ENST00000505634.1:c.329-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl transcript: ENST00000507659
  gene symbol: DCUN1D4
  hgvsc: ENST00000507659.1:n.230-32C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000425644
  ensembl transcript: ENST00000509376
  gene symbol: DCUN1D4
  hgvsc: ENST00000509376.1:c.*1041-2252C>G
  variant of: http://identifiers.org/hgnc/28998
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109184
  ensembl protein: ENSP00000423794
  ensembl transcript: ENST00000512199
  gene symbol: DCUN1D4
  hgvsc: ENST00000512199.1:c.*109-32C>G
  variant of: http://identifiers.org/hgnc/28998
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 236
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8544
bin: 7.5e0
variant carriers: 11

GenotypeDepth
all individuals: 16442
bin: 2.25e1
variant carriers: 13

GenotypeDepth
all individuals: 3984
bin: 3.75e1
variant carriers: 15

GenotypeDepth
all individuals: 94
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 94
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1193
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 8833
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15003
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 551
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2828
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1685
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1262
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 6210
bin: 9.75e1
variant carriers: 123

GenotypeQuality
all individuals: 3320
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1466
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 908
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 708
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5445
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1763
bin: 9.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.402384444695174e-5
allele num: 53178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.988643156007172e-4
allele num: 13384
num of homozygotes: 0

African
type: Population
allele count: 93
allele frequency: 1.295986622073579e-2
allele num: 7176
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.833516685001834e-3
allele num: 5454
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.495886312640239e-3
allele num: 10696
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.104e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

DP
type: SiteQuality
SIO_000300: 1.569108e6

VQSLOD
type: SiteQuality
SIO_000300: 5.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.207e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeDepth
all individuals: 6169
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 838
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11206
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 157
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4068
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7044
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6213
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 154
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7373
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15158
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.699928602998674e-5
allele num: 58826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

QD
type: SiteQuality
SIO_000300: 5.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.65834e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.531e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.07e0

GenotypeDepth
all individuals: 240
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 100
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 838
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 751
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4068
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7044
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6213
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7373
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 202
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15158
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.699928602998674e-5
allele num: 58826
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.65834e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.531e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

QD
type: SiteQuality
SIO_000300: 5.19e0

GenotypeDepth
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 838
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11621
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2602
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4044
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3506
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7372
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4951
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3350
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7406
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1826
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15508
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.941e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.541e1

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 1.693365e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.66e-1

GenotypeDepth
all individuals: 242
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 4317
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 838
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1249
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 103
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 402
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7438
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4382
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7619
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4234
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3440
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23712
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7870
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.8261253309797e-4
allele num: 11330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61084
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15680
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.24e-1

FS
type: SiteQuality
SIO_000300: 3.831e0

QD
type: SiteQuality
SIO_000300: 1.579e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.86e-1

DP
type: SiteQuality
SIO_000300: 1.70625e6

GenotypeDepth
all individuals: 292
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25335
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3597
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1860
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7944
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7452
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 208
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.583130164962163e-5
allele num: 63166
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.743226e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.02e-1

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 8.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.104e-1

MQ
type: SiteQuality
SIO_000300: 5.794e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.882e0

GenotypeDepth
all individuals: 243
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 578
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 21589
bin: 2.25e1
variant carriers: 8

GenotypeDepth
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1297
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 903
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 997
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7205
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 3716
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 941
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3266
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 2.5e0
variant carriers: 12

GenotypeQuality
all individuals: 6705
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1710
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 21000
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 485
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 955
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2588
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2042
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.096972356296621e-4
allele num: 9116
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.963786303334529e-5
allele num: 11156
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.335529650278763e-4
allele num: 7892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.623165822620439e-4
allele num: 61608
num of homozygotes: 0

South Asian
type: Population
allele count: 31
allele frequency: 2.124742974640164e-3
allele num: 14590
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

DP
type: SiteQuality
SIO_000300: 1.894201e6

FS
type: SiteQuality
SIO_000300: 1.015e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

QD
type: SiteQuality
SIO_000300: 3.06e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

GenotypeDepth
all individuals: 865
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3522
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1931
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21000
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6705
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1710
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3716
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2042
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7205
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11156
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.854009595613433e-5
allele num: 14590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

FS
type: SiteQuality
SIO_000300: 1.015e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 3.06e0

DP
type: SiteQuality
SIO_000300: 1.894201e6

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 3

GenotypeDepth
all individuals: 1297
bin: 5.25e1
variant carriers: 13

GenotypeDepth
all individuals: 865
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 274
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 578
bin: 6.25e1
variant carriers: 6

GenotypeDepth
all individuals: 243
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 842
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 462
bin: 1.75e1
variant carriers: 25

GenotypeQuality
all individuals: 2588
bin: 2.25e1
variant carriers: 18

GenotypeQuality
all individuals: 1428
bin: 2.5e0
variant carriers: 18

GenotypeQuality
all individuals: 941
bin: 4.25e1
variant carriers: 14

GenotypeQuality
all individuals: 966
bin: 3.75e1
variant carriers: 12

GenotypeQuality
all individuals: 903
bin: 2.75e1
variant carriers: 15

GenotypeQuality
all individuals: 997
bin: 3.25e1
variant carriers: 18

GenotypeQuality
all individuals: 485
bin: 1.25e1
variant carriers: 21

GenotypeQuality
all individuals: 856
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 619
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 21000
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6705
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3716
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2042
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3055
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 955
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 796
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1710
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3266
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7205
bin: 9.75e1
variant carriers: 27

African
type: Population
allele count: 2
allele frequency: 2.193944712593243e-4
allele num: 9116
num of homozygotes: 0

South Asian
type: Population
allele count: 36
allele frequency: 2.467443454420836e-3
allele num: 14590
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.585514521333812e-4
allele num: 11156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.544163063619518e-4
allele num: 6476
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.801317790167258e-4
allele num: 7892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 80
allele frequency: 1.298532658096351e-3
allele num: 61608
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.184834123222749e-3
allele num: 844
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.894201e6

QD
type: SiteQuality
SIO_000300: 3.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 1.015e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

GenotypeDepth
all individuals: 325
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22695
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9422
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 763
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1870
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3356
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 848
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8785
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518418415378542e-5
allele num: 65858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.619e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

FS
type: SiteQuality
SIO_000300: 4.302e0

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.78e-1

DP
type: SiteQuality
SIO_000300: 1.87758e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.523e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeDepth
all individuals: 23124
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13285
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1872
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3352
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 856
bin: 9.75e1
variant carriers: 8

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 108
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 9466
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8361
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2526
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25868
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8803
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 4523
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3962
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3779
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.415313084958638e-4
allele num: 66244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

DP
type: SiteQuality
SIO_000300: 1.888669e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

QD
type: SiteQuality
SIO_000300: 1.42e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

FS
type: SiteQuality
SIO_000300: 6.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4795
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9489
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 105
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2531
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3786
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8802
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 300
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4527
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8386
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3968
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165229550221394e-4
allele num: 8582
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66452
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.457000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.187e0

DP
type: SiteQuality
SIO_000300: 1.89274e6

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 8.300000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.959e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeDepth
all individuals: 1198
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 428
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26277
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4532
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8400
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3974
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8800
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3791
bin: 7.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.298e1

MQRankSum
type: SiteQuality
SIO_000300: 8.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e-1

DP
type: SiteQuality
SIO_000300: 1.894747e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

GenotypeDepth
all individuals: 13407
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 848
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3353
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1199
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4796
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 764
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3978
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26326
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3793
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4539
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8803
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8405
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212856276531231e-4
allele num: 16490
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.41e-1

DP
type: SiteQuality
SIO_000300: 1.895567e6

MQRankSum
type: SiteQuality
SIO_000300: -1.135e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.49e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

GenotypeDepth
all individuals: 1199
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13429
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23518
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26355
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3981
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 109
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3800
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8411
bin: 6.75e1
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: 15
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8803
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 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: 66630
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 6.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.28e0

VQSLOD
type: SiteQuality
SIO_000300: -1.703e0

DP
type: SiteQuality
SIO_000300: 1.89664e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.642e0

QD
type: SiteQuality
SIO_000300: 8.16e0

GenotypeDepth
all individuals: 154
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 105
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 848
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4798
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3802
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26371
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
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: 4541
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8414
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3984
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8803
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.7e-2

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

DP
type: SiteQuality
SIO_000300: 1.896865e6

GenotypeDepth
all individuals: 105
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1198
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 764
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 850
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4797
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3354
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9517
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 3985
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26398
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8804
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3804
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.898195e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.446e1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

FS
type: SiteQuality
SIO_000300: 3.247e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeDepth
all individuals: 850
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4798
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1876
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23527
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9522
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13466
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1198
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26385
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 8427
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3985
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4544
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8805
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2537
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 1.427e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.89803e6

QD
type: SiteQuality
SIO_000300: 9.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.328e0

VQSLOD
type: SiteQuality
SIO_000300: 6.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

GenotypeDepth
all individuals: 13492
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 84
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1198
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4796
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3809
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3984
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8436
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26362
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8804
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
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: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-1

FS
type: SiteQuality
SIO_000300: 1.265e0

VQSLOD
type: SiteQuality
SIO_000300: -1.748e0

DP
type: SiteQuality
SIO_000300: 1.898242e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.267e0

QD
type: SiteQuality
SIO_000300: 1.265e1

GenotypeDepth
all individuals: 429
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23459
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 849
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 765
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8805
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4556
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26307
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3806
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3984
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8448
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.972e0

DP
type: SiteQuality
SIO_000300: 1.89795e6

MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.202e0

QD
type: SiteQuality
SIO_000300: 6.86e0

VQSLOD
type: SiteQuality
SIO_000300: -2.275e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.82e-2

GenotypeQuality
all individuals: 2073
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25699
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3781
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8301
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4533
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3971
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8801
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.383e0

DP
type: SiteQuality
SIO_000300: 1.890113e6

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.359e1

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.071e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 2073
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25459
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4526
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3774
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8801
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.459e1

DP
type: SiteQuality
SIO_000300: 1.887141e6

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25459
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8801
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3774
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4526
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2073
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 1.459e1

DP
type: SiteQuality
SIO_000300: 1.887141e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 1.68e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8190
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8801
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25123
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2073
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4524
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.949e0

QD
type: SiteQuality
SIO_000300: 1.078e1

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

FS
type: SiteQuality
SIO_000300: 4.808e0

DP
type: SiteQuality
SIO_000300: 1.884349e6

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24324
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3728
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8802
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 340
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8004
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4514
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3956
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003724618526973e-5
allele num: 66584
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.601e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e0

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.397e0

VQSLOD
type: SiteQuality
SIO_000300: 4.37e-1

QD
type: SiteQuality
SIO_000300: 1.436e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.738e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.877646e6

GenotypeQuality
all individuals: 2534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8804
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3952
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 24448
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 344
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2071
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 1.428e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.877445e6

GenotypeQuality
all individuals: 345
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4510
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3717
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7998
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2071
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8807
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3952
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24647
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.925669170036588e-4
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.51e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.328e1

DP
type: SiteQuality
SIO_000300: 1.877251e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 4.985e0

VQSLOD
type: SiteQuality
SIO_000300: -1.208e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.83e-1

GenotypeQuality
all individuals: 4486
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2070
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7703
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8806
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3950
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21452
bin: 6.25e1
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: 10364
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.147792942333702e-5
allele num: 16266
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: 8602
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.457e1

DP
type: SiteQuality
SIO_000300: 1.859636e6

FS
type: SiteQuality
SIO_000300: 3.882e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.736e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -7.944e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.803e0

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3950
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4479
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19284
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2538
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8809
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3648
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7521
bin: 6.75e1
variant carriers: 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: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.520114509567576e-5
allele num: 66370
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: 16146
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.767e0

DP
type: SiteQuality
SIO_000300: 1.862829e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

QD
type: SiteQuality
SIO_000300: 1.233e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.392e0

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.74e-1

GenotypeQuality
all individuals: 5836
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 905
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6673
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6370
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2818
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4643
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4621
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5034
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.676e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

DP
type: SiteQuality
SIO_000300: 7.83208e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.42e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2180
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20736
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24812
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 470
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 3
allele frequency: 4.542701393095094e-4
allele num: 6604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 1.134816159782115e-4
allele num: 8812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36944
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.196e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 4.166e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 1.08231e6

GenotypeQuality
all individuals: 2000
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 350
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20015
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2313
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 395
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26080
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 692
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.249619402593312e-5
allele num: 38098
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6742
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5118
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: 5.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.077e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

QD
type: SiteQuality
SIO_000300: 1.077e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

DP
type: SiteQuality
SIO_000300: 1.101085e6

GenotypeQuality
all individuals: 100
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 257
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1658
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18758
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.505637684790779e-5
allele num: 39910
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

QD
type: SiteQuality
SIO_000300: 5.53e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.592e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.645e0

DP
type: SiteQuality
SIO_000300: 1.133674e6

GenotypeDepth
all individuals: 165
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12395
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 555
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 34543
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 2.49500998003992e-4
allele num: 8016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7608
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 7.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.891e-1

FS
type: SiteQuality
SIO_000300: 4.187e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.271722e6

GenotypeDepth
all individuals: 891
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11581
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37165
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.88041832943443e-5
allele num: 14534
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51006
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.134e1

DP
type: SiteQuality
SIO_000300: 1.291118e6

MQ
type: SiteQuality
SIO_000300: 5.861e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

FS
type: SiteQuality
SIO_000300: 7.952e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.556e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

GenotypeDepth
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10913
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2350
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 565
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2732
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.19161105815062e-4
allele num: 8392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.103e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.203e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.73e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.851e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.73e-1

DP
type: SiteQuality
SIO_000300: 1.306188e6

GenotypeDepth
all individuals: 124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2664
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37381
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11072
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 615
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2352
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 558
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 3.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.890859584767235e-5
allele num: 52886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5932
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 4.591e0

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.312354e6

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeDepth
all individuals: 122
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2352
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5880
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.916736947021391e-5
allele num: 52172
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.227e-1

QD
type: SiteQuality
SIO_000300: 6.44e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

FS
type: SiteQuality
SIO_000300: 1.129e0

DP
type: SiteQuality
SIO_000300: 1.292318e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -9.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

GenotypeDepth
all individuals: 516
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2608
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2361
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 814
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12822
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14676
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51896
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.551098376313276e-5
allele num: 10470
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.283677e6

FS
type: SiteQuality
SIO_000300: 1.104e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 165
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 402
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12822
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2608
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2361
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 511
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 9
allele frequency: 1.04384133611691e-3
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.104e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

VQSLOD
type: SiteQuality
SIO_000300: 4.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

DP
type: SiteQuality
SIO_000300: 1.283677e6

GenotypeDepth
all individuals: 190
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32857
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1306
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2539
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13174
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2353
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 681
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.831534362617844e-5
allele num: 14638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10454
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51626
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

DP
type: SiteQuality
SIO_000300: 1.276849e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.47e-1

FS
type: SiteQuality
SIO_000300: 1.534e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 1.122e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.38e-1

GenotypeDepth
all individuals: 2015
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33018
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2353
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 558
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 2.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.956105003716599e-5
allele num: 51122
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.127e1

FS
type: SiteQuality
SIO_000300: 3.969e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

DP
type: SiteQuality
SIO_000300: 1.264032e6

GenotypeDepth
all individuals: 1534
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 517
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2354
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31264
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.383891502906172e-4
allele num: 14452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 9.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.604e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

DP
type: SiteQuality
SIO_000300: 1.243809e6

VQSLOD
type: SiteQuality
SIO_000300: -2.747e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e-1

GenotypeDepth
all individuals: 112
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 123
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 516
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16706
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1587
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2367
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 29148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.71591526344378e-4
allele num: 7364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.219979818365288e-4
allele num: 49550
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.1936022917164e-4
allele num: 8378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14352
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 1.04e1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 6.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.115e0

DP
type: SiteQuality
SIO_000300: 1.218914e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

GenotypeDepth
all individuals: 122
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 516
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1733
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2354
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29126
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2354
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17023
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.026917463920869e-5
allele num: 49336
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

QD
type: SiteQuality
SIO_000300: 8.199999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.215657e6

VQSLOD
type: SiteQuality
SIO_000300: 9.49e-1

GenotypeDepth
all individuals: 26271
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 190
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17531
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2361
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 749
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27677
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.040316657145189e-5
allele num: 49012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7266
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.971473851030111e-4
allele num: 10096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.794466955428252e-4
allele num: 14314
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 1.20601e6

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

QD
type: SiteQuality
SIO_000300: 1.034e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.205e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

GenotypeDepth
all individuals: 24876
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1853
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26483
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18583
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 696
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.066030329325234e-5
allele num: 48402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.69e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

DP
type: SiteQuality
SIO_000300: 1.186642e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

FS
type: SiteQuality
SIO_000300: 1.091e1

VQSLOD
type: SiteQuality
SIO_000300: -1.342e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeDepth
all individuals: 125
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1513
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20767
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 382
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7002
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.11999152003392e-5
allele num: 47170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 3.931e0

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

DP
type: SiteQuality
SIO_000300: 1.148303e6

QD
type: SiteQuality
SIO_000300: 6.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.314e0

VQSLOD
type: SiteQuality
SIO_000300: -1.057e0

GenotypeDepth
all individuals: 21028
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2506
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 516
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21201
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.140319335644878e-5
allele num: 46722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.345e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.268e0

VQSLOD
type: SiteQuality
SIO_000300: -2.152e0

DP
type: SiteQuality
SIO_000300: 1.13743e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

MQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

FS
type: SiteQuality
SIO_000300: 1.3497e1

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24155
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17475
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2877
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1917
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1169
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3264
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.243963737546001e-5
allele num: 44564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5370
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

DP
type: SiteQuality
SIO_000300: 1.06799e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.602e1

FS
type: SiteQuality
SIO_000300: 1.996e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.487e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.503e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.68e-1

GenotypeDepth
all individuals: 125
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15869
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24896
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2362
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13760
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.592000734720118e-5
allele num: 43554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.099384344766931e-4
allele num: 9096
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.301066874837367e-4
allele num: 7686
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.106e0

QD
type: SiteQuality
SIO_000300: 1.252e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 1.042891e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

GenotypeDepth
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11424
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4288
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25429
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 166
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4180
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6164
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.446016381236039e-5
allele num: 13430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.124e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.537e0

DP
type: SiteQuality
SIO_000300: 9.76604e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4806
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2421
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6357
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2583
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4384
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7451
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3200
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4926
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.243162605668821e-4
allele num: 8044
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5652
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.352e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.203e0

DP
type: SiteQuality
SIO_000300: 9.22638e5

GenotypeDepth
all individuals: 126
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 519
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4691
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21821
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7820
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2570
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6474
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4312
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 295
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 14
allele frequency: 1.080080234531708e-3
allele num: 12962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36660
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-2

QD
type: SiteQuality
SIO_000300: 1.079e1

DP
type: SiteQuality
SIO_000300: 9.2024e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.573e0

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.612e0

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1157
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 441
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 457
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.336183858898984e-4
allele num: 7484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2698
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.89e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.056e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.069e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e0

QD
type: SiteQuality
SIO_000300: 1.135e1

MQ
type: SiteQuality
SIO_000300: 4.934e1

DP
type: SiteQuality
SIO_000300: 1.83522e5

GenotypeDepth
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1459
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2057
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.84561e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -8.761e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

QD
type: SiteQuality
SIO_000300: 1.339e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.77e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2162
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 263
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 473
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.245e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.042e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 1.88179e5

QD
type: SiteQuality
SIO_000300: 1.006e1

MQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2068
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2742
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.997867803837953e-4
allele num: 7504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2722
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.77e-2

DP
type: SiteQuality
SIO_000300: 1.89887e5

QD
type: SiteQuality
SIO_000300: 9.33e0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 684
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 607
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2931
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332977872567315e-4
allele num: 7502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2722
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.027e0

MQRankSum
type: SiteQuality
SIO_000300: -4.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: -1.798e0

DP
type: SiteQuality
SIO_000300: 1.90376e5

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.08e-2

FS
type: SiteQuality
SIO_000300: 1.063e0

QD
type: SiteQuality
SIO_000300: 1.739e1

GenotypeDepth
all individuals: 590
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 651
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 248
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332622601279318e-4
allele num: 7504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

DP
type: SiteQuality
SIO_000300: 2.07466e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.827e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.23e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.574e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.816e0

GenotypeDepth
all individuals: 801
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 419
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332622601279318e-4
allele num: 7504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.363e0

VQSLOD
type: SiteQuality
SIO_000300: -5.639e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.78e-1

QD
type: SiteQuality
SIO_000300: 1.156e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.23e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

DP
type: SiteQuality
SIO_000300: 2.07608e5

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332622601279318e-4
allele num: 7504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.125e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.614e0

FS
type: SiteQuality
SIO_000300: 7.702e0

MQRankSum
type: SiteQuality
SIO_000300: -1.712e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

DP
type: SiteQuality
SIO_000300: 2.07446e5

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 418
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2719
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2331
bin: 9.75e1
variant carriers: 4

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

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

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

GenotypeQuality
all individuals: 306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.330490405117271e-4
allele num: 7504
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.744e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.15e1

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

DP
type: SiteQuality
SIO_000300: 2.07746e5

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2765
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 306
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332622601279318e-4
allele num: 7504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

FS
type: SiteQuality
SIO_000300: 1.527e0

MQRankSum
type: SiteQuality
SIO_000300: -1.195e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.86e-1

DP
type: SiteQuality
SIO_000300: 2.07663e5

VQSLOD
type: SiteQuality
SIO_000300: -2.352e0

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.29e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

GenotypeDepth
all individuals: 592
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 340
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 429
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 131
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2675
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2740
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332622601279318e-4
allele num: 7504
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.76e1

FS
type: SiteQuality
SIO_000300: 9.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.536e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

DP
type: SiteQuality
SIO_000300: 2.07457e5

GenotypeDepth
all individuals: 1268
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1452
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14413
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2796
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 438
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14644
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2428
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4552
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3611
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22547
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

DP
type: SiteQuality
SIO_000300: 2.256997e6