10-124339105-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339105
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339105
    reference: chr 10
allele count: 10
allele frequency: 8.2847295864263e-5
allele num: 120704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1277A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.691A>G
  hgvsp: ENSP00000357952.2:p.Ser231Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.691A>G
  hgvsp: ENSP00000327747.4:p.Ser231Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.691A>G
  hgvsp: ENSP00000343175.3:p.Ser231Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.691A>G
  hgvsp: ENSP00000357951.3:p.Ser231Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.691A>G
  hgvsp: ENSP00000342210.3:p.Ser231Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.691A>G
  hgvsp: ENSP00000357905.3:p.Ser231Gly
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39688
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52628
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser231Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

10-124339106-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339106
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339106
    reference: chr 10
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.692G>C
  hgvsp: ENSP00000327747.4:p.Ser231Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.692G>C
  hgvsp: ENSP00000357951.3:p.Ser231Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.692G>C
  hgvsp: ENSP00000357905.3:p.Ser231Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.692G>C
  hgvsp: ENSP00000343175.3:p.Ser231Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1276G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.692G>C
  hgvsp: ENSP00000342210.3:p.Ser231Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.692G>C
  hgvsp: ENSP00000357952.2:p.Ser231Thr
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39687
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser231Thr
num of homozygotes: 1
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

10-124339110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339110
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339110
    reference: chr 10
allele count: 3
allele frequency: 2.484101748807631e-5
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.696G>A
  hgvsp: ENST00000368909.3:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.696G>A
  hgvsp: ENST00000344338.3:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.696G>A
  hgvsp: ENST00000368955.3:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1272G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.696G>A
  hgvsp: ENST00000368956.2:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.696G>A
  hgvsp: ENST00000330163.4:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.696G>A
  hgvsp: ENST00000338354.3:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39687
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3386
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52659
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu232Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

10-124339113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339113
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339113
    reference: chr 10
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.699C>T
  hgvsp: ENST00000338354.3:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.699C>T
  hgvsp: ENST00000330163.4:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1269C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.699C>T
  hgvsp: ENST00000368955.3:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.699C>T
  hgvsp: ENST00000344338.3:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.699C>T
  hgvsp: ENST00000368956.2:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.699C>T
  hgvsp: ENST00000368909.3:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39686
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala233Ala
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-124339119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339119
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339119
    reference: chr 10
allele count: 58
allele frequency: 4.80259671436142e-4
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.705G>A
  hgvsp: ENST00000368956.2:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.705G>A
  hgvsp: ENST00000368955.3:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.705G>A
  hgvsp: ENST00000330163.4:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.705G>A
  hgvsp: ENST00000344338.3:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1263G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.705G>A
  hgvsp: ENST00000368909.3:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.705G>A
  hgvsp: ENST00000338354.3:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39691
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg235Arg
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

10-124339125-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339125
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339125
    reference: chr 10
allele count: 3
allele frequency: 2.484101748807631e-5
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.711G>C
  hgvsp: ENST00000368909.3:c.711G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.711G>C
  hgvsp: ENST00000338354.3:c.711G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.711G>C
  hgvsp: ENST00000330163.4:c.711G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.711G>C
  hgvsp: ENST00000368955.3:c.711G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.711G>C
  hgvsp: ENST00000344338.3:c.711G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.711G>C
  hgvsp: ENST00000368956.2:c.711G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1257G>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39685
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val237Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

10-124339129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339129
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339129
    reference: chr 10
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.715G>A
  hgvsp: ENSP00000343175.3:p.Gly239Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1253G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.715G>A
  hgvsp: ENSP00000357905.3:p.Gly239Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.715G>A
  hgvsp: ENSP00000342210.3:p.Gly239Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.715G>A
  hgvsp: ENSP00000357952.2:p.Gly239Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.715G>A
  hgvsp: ENSP00000357951.3:p.Gly239Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.715G>A
  hgvsp: ENSP00000327747.4:p.Gly239Arg
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39684
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly239Arg
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

10-124339133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339133
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339133
    reference: chr 10
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.719G>A
  hgvsp: ENSP00000342210.3:p.Gly240Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.719G>A
  hgvsp: ENSP00000327747.4:p.Gly240Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.719G>A
  hgvsp: ENSP00000343175.3:p.Gly240Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1249G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.719G>A
  hgvsp: ENSP00000357905.3:p.Gly240Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.719G>A
  hgvsp: ENSP00000357951.3:p.Gly240Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.719G>A
  hgvsp: ENSP00000357952.2:p.Gly240Asp
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39685
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly240Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

10-124339134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339134
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339134
    reference: chr 10
allele count: 17
allele frequency: 1.407657657657658e-4
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.720C>T
  hgvsp: ENST00000344338.3:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.720C>T
  hgvsp: ENST00000368909.3:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.720C>T
  hgvsp: ENST00000368956.2:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.720C>T
  hgvsp: ENST00000330163.4:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.720C>T
  hgvsp: ENST00000368955.3:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.720C>T
  hgvsp: ENST00000338354.3:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1248C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39685
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly240Gly
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

10-124339135-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339135
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339135
    reference: chr 10
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.721G>A
  hgvsp: ENSP00000357951.3:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.721G>A
  hgvsp: ENSP00000327747.4:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.721G>A
  hgvsp: ENSP00000342210.3:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.721G>A
  hgvsp: ENSP00000357905.3:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.721G>A
  hgvsp: ENSP00000357952.2:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.721G>A
  hgvsp: ENSP00000343175.3:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1247G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp241Asn
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

10-124339135-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339135
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339135
    reference: chr 10
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.721G>C
  hgvsp: ENSP00000357905.3:p.Asp241His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.721G>C
  hgvsp: ENSP00000357951.3:p.Asp241His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.721G>C
  hgvsp: ENSP00000342210.3:p.Asp241His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.721G>C
  hgvsp: ENSP00000327747.4:p.Asp241His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.721G>C
  hgvsp: ENSP00000357952.2:p.Asp241His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1247G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.721G>C
  hgvsp: ENSP00000343175.3:p.Asp241His
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp241His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-124339137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339137
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339137
    reference: chr 10
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.723C>T
  hgvsp: ENST00000330163.4:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.723C>T
  hgvsp: ENST00000344338.3:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1245C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.723C>T
  hgvsp: ENST00000368955.3:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.723C>T
  hgvsp: ENST00000368909.3:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.723C>T
  hgvsp: ENST00000368956.2:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.723C>T
  hgvsp: ENST00000338354.3:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3375
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52681
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp241Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

10-124339138-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339138
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339138
    reference: chr 10
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1244A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.724A>G
  hgvsp: ENSP00000357905.3:p.Arg242Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.724A>G
  hgvsp: ENSP00000327747.4:p.Arg242Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.724A>G
  hgvsp: ENSP00000357951.3:p.Arg242Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.724A>G
  hgvsp: ENSP00000342210.3:p.Arg242Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.724A>G
  hgvsp: ENSP00000343175.3:p.Arg242Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.724A>G
  hgvsp: ENSP00000357952.2:p.Arg242Gly
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52681
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg242Gly
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

10-124339145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339145
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339145
    reference: chr 10
allele count: 32
allele frequency: 2.649664651817504e-4
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.731G>A
  hgvsp: ENSP00000357952.2:p.Arg244Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.731G>A
  hgvsp: ENSP00000343175.3:p.Arg244Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.731G>A
  hgvsp: ENSP00000357905.3:p.Arg244Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.731G>A
  hgvsp: ENSP00000342210.3:p.Arg244Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.731G>A
  hgvsp: ENSP00000357951.3:p.Arg244Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1237G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.731G>A
  hgvsp: ENSP00000327747.4:p.Arg244Gln
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 39677
  bin: 9.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg244Gln
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

10-124339146-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339146
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339146
    reference: chr 10
allele count: 14
allele frequency: 1.159228285170158e-4
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.732A>G
  hgvsp: ENST00000368955.3:c.732A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.732A>G
  hgvsp: ENST00000344338.3:c.732A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1236A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.732A>G
  hgvsp: ENST00000330163.4:c.732A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.732A>G
  hgvsp: ENST00000368909.3:c.732A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.732A>G
  hgvsp: ENST00000338354.3:c.732A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.732A>G
  hgvsp: ENST00000368956.2:c.732A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39669
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3378
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg244Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum

10-124339149-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339149
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339149
    reference: chr 10
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.735C>T
  hgvsp: ENST00000368955.3:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.735C>T
  hgvsp: ENST00000338354.3:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.735C>T
  hgvsp: ENST00000368956.2:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.735C>T
  hgvsp: ENST00000344338.3:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.735C>T
  hgvsp: ENST00000368909.3:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.735C>T
  hgvsp: ENST00000330163.4:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1233C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52679
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly245Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

10-124339150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339150
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339150
    reference: chr 10
allele count: 144
allele frequency: 1.192349093317877e-3
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1232C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.736C>T
  hgvsp: ENSP00000357905.3:p.Arg246Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.736C>T
  hgvsp: ENSP00000357951.3:p.Arg246Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.736C>T
  hgvsp: ENSP00000327747.4:p.Arg246Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.736C>T
  hgvsp: ENSP00000343175.3:p.Arg246Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.736C>T
  hgvsp: ENSP00000357952.2:p.Arg246Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.736C>T
  hgvsp: ENSP00000342210.3:p.Arg246Ter
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39669
  bin: 9.75e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg246Ter
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

10-124339151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339151
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339151
    reference: chr 10
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.737G>A
  hgvsp: ENSP00000327747.4:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.737G>A
  hgvsp: ENSP00000357951.3:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.737G>A
  hgvsp: ENSP00000357952.2:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.737G>A
  hgvsp: ENSP00000342210.3:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1231G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.737G>A
  hgvsp: ENSP00000343175.3:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.737G>A
  hgvsp: ENSP00000357905.3:p.Arg246Gln
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39624
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3378
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52677
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg246Gln
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS

10-124339151-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339151
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339151
    reference: chr 10
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.737G>T
  hgvsp: ENSP00000343175.3:p.Arg246Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.737G>T
  hgvsp: ENSP00000357951.3:p.Arg246Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.737G>T
  hgvsp: ENSP00000342210.3:p.Arg246Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.737G>T
  hgvsp: ENSP00000357905.3:p.Arg246Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1231G>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.737G>T
  hgvsp: ENSP00000357952.2:p.Arg246Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.737G>T
  hgvsp: ENSP00000327747.4:p.Arg246Leu
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39624
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3378
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg246Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

10-124339155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339155
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339155
    reference: chr 10
allele count: 11
allele frequency: 9.108222240622672e-5
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.741G>A
  hgvsp: ENST00000344338.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.741G>A
  hgvsp: ENST00000368909.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.741G>A
  hgvsp: ENST00000338354.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.741G>A
  hgvsp: ENST00000330163.4:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1227G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.741G>A
  hgvsp: ENST00000368955.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.741G>A
  hgvsp: ENST00000368956.2:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39623
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3379
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val247Val
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

10-124339159-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339159
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339159
    reference: chr 10
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.745G>T
  hgvsp: ENSP00000357951.3:p.Val249Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.745G>T
  hgvsp: ENSP00000357952.2:p.Val249Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.745G>T
  hgvsp: ENSP00000327747.4:p.Val249Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.745G>T
  hgvsp: ENSP00000343175.3:p.Val249Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.745G>T
  hgvsp: ENSP00000342210.3:p.Val249Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1223G>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.745G>T
  hgvsp: ENSP00000357905.3:p.Val249Phe
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39619
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52675
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val249Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-124339162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339162
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339162
    reference: chr 10
allele count: 13
allele frequency: 1.076461918089529e-4
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.748C>T
  hgvsp: ENST00000344338.3:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.748C>T
  hgvsp: ENST00000338354.3:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.748C>T
  hgvsp: ENST00000368909.3:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.748C>T
  hgvsp: ENST00000330163.4:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.748C>T
  hgvsp: ENST00000368955.3:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.748C>T
  hgvsp: ENST00000368956.2:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1220C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39620
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3375
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu250Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

10-124339165-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339165
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339165
    reference: chr 10
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1217T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.751T>C
  hgvsp: ENSP00000327747.4:p.Tyr251His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.751T>C
  hgvsp: ENSP00000357952.2:p.Tyr251His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.751T>C
  hgvsp: ENSP00000343175.3:p.Tyr251His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.751T>C
  hgvsp: ENSP00000357951.3:p.Tyr251His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.751T>C
  hgvsp: ENSP00000342210.3:p.Tyr251His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.751T>C
  hgvsp: ENSP00000357905.3:p.Tyr251His
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr251His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

10-124339167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339167
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339167
    reference: chr 10
allele count: 15
allele frequency: 1.242071443949456e-4
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.753C>T
  hgvsp: ENST00000344338.3:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.753C>T
  hgvsp: ENST00000338354.3:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.753C>T
  hgvsp: ENST00000368909.3:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.753C>T
  hgvsp: ENST00000330163.4:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.753C>T
  hgvsp: ENST00000368956.2:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1215C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.753C>T
  hgvsp: ENST00000368955.3:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39617
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr251Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

10-124339169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339169
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339169
    reference: chr 10
allele count: 12
allele frequency: 9.936571551595648e-5
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.755G>A
  hgvsp: ENSP00000327747.4:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.755G>A
  hgvsp: ENSP00000357905.3:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.755G>A
  hgvsp: ENSP00000343175.3:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.755G>A
  hgvsp: ENSP00000342210.3:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.755G>A
  hgvsp: ENSP00000357951.3:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.755G>A
  hgvsp: ENSP00000357952.2:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1213G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39612
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3373
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52677
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg252Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

10-124339171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339171
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339171
    reference: chr 10
allele count: 69
allele frequency: 5.713528642167497e-4
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.757G>A
  hgvsp: ENSP00000357905.3:p.Gly253Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.757G>A
  hgvsp: ENSP00000357952.2:p.Gly253Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.757G>A
  hgvsp: ENSP00000343175.3:p.Gly253Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.757G>A
  hgvsp: ENSP00000357951.3:p.Gly253Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.757G>A
  hgvsp: ENSP00000327747.4:p.Gly253Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.757G>A
  hgvsp: ENSP00000342210.3:p.Gly253Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1211G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39625
  bin: 9.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly253Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

10-124339181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339181
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339181
    reference: chr 10
allele count: 2
allele frequency: 1.656314699792961e-5
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.767G>A
  hgvsp: ENSP00000357905.3:p.Gly256Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.767G>A
  hgvsp: ENSP00000342210.3:p.Gly256Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.767G>A
  hgvsp: ENSP00000357951.3:p.Gly256Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.767G>A
  hgvsp: ENSP00000357952.2:p.Gly256Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.767G>A
  hgvsp: ENSP00000327747.4:p.Gly256Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.767G>A
  hgvsp: ENSP00000343175.3:p.Gly256Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1201G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39611
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly256Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-124339182-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339182
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339182
    reference: chr 10
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1200C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.768C>A
  hgvsp: ENST00000368955.3:c.768C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.768C>A
  hgvsp: ENST00000368956.2:c.768C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.768C>A
  hgvsp: ENST00000344338.3:c.768C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.768C>A
  hgvsp: ENST00000368909.3:c.768C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.768C>A
  hgvsp: ENST00000330163.4:c.768C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.768C>A
  hgvsp: ENST00000338354.3:c.768C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39612
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3330
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly256Gly
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-124339182-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339182
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339182
    reference: chr 10
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.768C>T
  hgvsp: ENST00000330163.4:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.768C>T
  hgvsp: ENST00000368955.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.768C>T
  hgvsp: ENST00000368956.2:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.768C>T
  hgvsp: ENST00000344338.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.768C>T
  hgvsp: ENST00000368909.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1200C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.768C>T
  hgvsp: ENST00000338354.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39612
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52704
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly256Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-124339184-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339184
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339184
    reference: chr 10
allele count: 21
allele frequency: 1.739188047637189e-4
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.770C>A
  hgvsp: ENSP00000342210.3:p.Thr257Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.770C>A
  hgvsp: ENSP00000357952.2:p.Thr257Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1198C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.770C>A
  hgvsp: ENSP00000357951.3:p.Thr257Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.770C>A
  hgvsp: ENSP00000327747.4:p.Thr257Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.770C>A
  hgvsp: ENSP00000343175.3:p.Thr257Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.770C>A
  hgvsp: ENSP00000357905.3:p.Thr257Asn
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39612
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr257Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

10-124339185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339185
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339185
    reference: chr 10
allele count: 2
allele frequency: 1.656397005234214e-5
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1197C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.771C>T
  hgvsp: ENST00000330163.4:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.771C>T
  hgvsp: ENST00000368955.3:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.771C>T
  hgvsp: ENST00000368909.3:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.771C>T
  hgvsp: ENST00000344338.3:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.771C>T
  hgvsp: ENST00000338354.3:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.771C>T
  hgvsp: ENST00000368956.2:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39606
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr257Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS

10-124339186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339186
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339186
    reference: chr 10
allele count: 3
allele frequency: 2.484636663298604e-5
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.772G>A
  hgvsp: ENSP00000327747.4:p.Val258Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.772G>A
  hgvsp: ENSP00000343175.3:p.Val258Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.772G>A
  hgvsp: ENSP00000342210.3:p.Val258Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.772G>A
  hgvsp: ENSP00000357951.3:p.Val258Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.772G>A
  hgvsp: ENSP00000357905.3:p.Val258Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.772G>A
  hgvsp: ENSP00000357952.2:p.Val258Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1196G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39606
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52704
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val258Met
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

10-124339191-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339191
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339191
    reference: chr 10
allele count: 320
allele frequency: 2.650366910169127e-3
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.777T>C
  hgvsp: ENST00000344338.3:c.777T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.777T>C
  hgvsp: ENST00000330163.4:c.777T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1191T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.777T>C
  hgvsp: ENST00000338354.3:c.777T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.777T>C
  hgvsp: ENST00000368909.3:c.777T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.777T>C
  hgvsp: ENST00000368955.3:c.777T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.777T>C
  hgvsp: ENST00000368956.2:c.777T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 39634
  bin: 9.75e1
  variant carriers: 211
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3246
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys259Cys
num of homozygotes: 5
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

10-124339194-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339194
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339194
    reference: chr 10
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.780T>C
  hgvsp: ENST00000338354.3:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.780T>C
  hgvsp: ENST00000368956.2:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.780T>C
  hgvsp: ENST00000344338.3:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1188T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.780T>C
  hgvsp: ENST00000330163.4:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.780T>C
  hgvsp: ENST00000368909.3:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.780T>C
  hgvsp: ENST00000368955.3:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39630
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp260Asp
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/10-124339196-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339196
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339195
    reference: chr 10
allele count: 12
allele frequency: 9.939040551285449e-5
allele num: 120736
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.783delC
  hgvsp: ENSP00000357905.3:p.Tyr262ThrfsTer102
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.783delC
  hgvsp: ENSP00000342210.3:p.Tyr262ThrfsTer102
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.783delC
  hgvsp: ENSP00000327747.4:p.Tyr262ThrfsTer102
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.783delC
  hgvsp: ENSP00000343175.3:p.Tyr262ThrfsTer102
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1185delC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.783delC
  hgvsp: ENSP00000357951.3:p.Tyr262ThrfsTer102
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.783delC
  hgvsp: ENSP00000357952.2:p.Tyr262ThrfsTer102
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 39630
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr262ThrfsTer102
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: AC
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

10-124339197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339197
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339197
    reference: chr 10
allele count: 68
allele frequency: 5.651971540660949e-4
allele num: 120312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.783C>T
  hgvsp: ENST00000368955.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.783C>T
  hgvsp: ENST00000330163.4:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.783C>T
  hgvsp: ENST00000368956.2:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.783C>T
  hgvsp: ENST00000338354.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.783C>T
  hgvsp: ENST00000344338.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.783C>T
  hgvsp: ENST00000368909.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1185C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39839
  bin: 9.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 52607
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 6
hgvs: p.Asp261Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

10-124339198-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339198
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339198
    reference: chr 10
allele count: 321
allele frequency: 2.659221949764729e-3
allele num: 120712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.784T>A
  hgvsp: ENSP00000343175.3:p.Tyr262Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.784T>A
  hgvsp: ENSP00000357952.2:p.Tyr262Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.784T>A
  hgvsp: ENSP00000327747.4:p.Tyr262Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.784T>A
  hgvsp: ENSP00000342210.3:p.Tyr262Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.784T>A
  hgvsp: ENSP00000357951.3:p.Tyr262Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.784T>A
  hgvsp: ENSP00000357905.3:p.Tyr262Asn
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1184T>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39695
  bin: 9.75e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 7.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53041
  bin: 9.75e1
  variant carriers: 316
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr262Asn
num of homozygotes: 5
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

10-124339199-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339199
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339200
    reference: chr 10
allele count: 12
allele frequency: 9.939040551285449e-5
allele num: 120736
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1183_608-1182insG
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.785_786insG
  hgvsp: ENSP00000357952.2:p.Tyr262Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.785_786insG
  hgvsp: ENSP00000357905.3:p.Tyr262Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.785_786insG
  hgvsp: ENSP00000327747.4:p.Tyr262Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.785_786insG
  hgvsp: ENSP00000343175.3:p.Tyr262Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.785_786insG
  hgvsp: ENSP00000342210.3:p.Tyr262Ter
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.785_786insG
  hgvsp: ENSP00000357951.3:p.Tyr262Ter
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39696
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr262Ter
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

10-124339199-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339199
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339199
    reference: chr 10
allele count: 322
allele frequency: 2.666975881261596e-3
allele num: 120736
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.785A>G
  hgvsp: ENSP00000357952.2:p.Tyr262Cys
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.785A>G
  hgvsp: ENSP00000342210.3:p.Tyr262Cys
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.785A>G
  hgvsp: ENSP00000343175.3:p.Tyr262Cys
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.785A>G
  hgvsp: ENSP00000327747.4:p.Tyr262Cys
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.785A>G
  hgvsp: ENSP00000357905.3:p.Tyr262Cys
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.785A>G
  hgvsp: ENSP00000357951.3:p.Tyr262Cys
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1183A>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 39696
  bin: 9.75e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3150
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr262Cys
num of homozygotes: 5
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

10-124339208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339208
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339208
    reference: chr 10
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.794C>T
  hgvsp: ENSP00000357905.3:p.Thr265Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.794C>T
  hgvsp: ENSP00000342210.3:p.Thr265Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.794C>T
  hgvsp: ENSP00000343175.3:p.Thr265Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.794C>T
  hgvsp: ENSP00000327747.4:p.Thr265Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1174C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.794C>T
  hgvsp: ENSP00000357952.2:p.Thr265Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.794C>T
  hgvsp: ENSP00000357951.3:p.Thr265Ile
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39643
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53049
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr265Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

10-124339211-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339211
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339211
    reference: chr 10
allele count: 13
allele frequency: 1.077032692084638e-4
allele num: 120702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.797A>G
  hgvsp: ENSP00000342210.3:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.797A>G
  hgvsp: ENSP00000357951.3:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.797A>G
  hgvsp: ENSP00000357905.3:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.797A>G
  hgvsp: ENSP00000343175.3:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1171A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.797A>G
  hgvsp: ENSP00000357952.2:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.797A>G
  hgvsp: ENSP00000327747.4:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39643
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3114
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn266Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-124339215-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339215
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339215
    reference: chr 10
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.801T>C
  hgvsp: ENST00000368956.2:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.801T>C
  hgvsp: ENST00000368909.3:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.801T>C
  hgvsp: ENST00000368955.3:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.801T>C
  hgvsp: ENST00000330163.4:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.801T>C
  hgvsp: ENST00000338354.3:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.801T>C
  hgvsp: ENST00000344338.3:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1167T>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39636
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp267Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

10-124339216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339216
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339216
    reference: chr 10
allele count: 3
allele frequency: 2.48541887592789e-5
allele num: 120704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.802G>A
  hgvsp: ENSP00000343175.3:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1166G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.802G>A
  hgvsp: ENSP00000357952.2:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.802G>A
  hgvsp: ENSP00000342210.3:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.802G>A
  hgvsp: ENSP00000357951.3:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.802G>A
  hgvsp: ENSP00000357905.3:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.802G>A
  hgvsp: ENSP00000327747.4:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39635
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala268Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

10-124339217-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339217
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339217
    reference: chr 10
allele count: 225
allele frequency: 1.864218602416027e-3
allele num: 120694
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.803C>T
  hgvsp: ENSP00000357905.3:p.Ala268Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.803C>T
  hgvsp: ENSP00000343175.3:p.Ala268Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.803C>T
  hgvsp: ENSP00000357952.2:p.Ala268Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.803C>T
  hgvsp: ENSP00000327747.4:p.Ala268Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.803C>T
  hgvsp: ENSP00000357951.3:p.Ala268Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.803C>T
  hgvsp: ENSP00000342210.3:p.Ala268Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1165C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39636
  bin: 9.75e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala268Val
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

10-124339221-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339221
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339221
    reference: chr 10
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1161T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.807T>C
  hgvsp: ENST00000330163.4:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.807T>C
  hgvsp: ENST00000368909.3:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.807T>C
  hgvsp: ENST00000338354.3:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.807T>C
  hgvsp: ENST00000344338.3:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.807T>C
  hgvsp: ENST00000368956.2:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.807T>C
  hgvsp: ENST00000368955.3:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53040
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn269Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

10-124339222-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339222
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339222
    reference: chr 10
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.808G>A
  hgvsp: ENSP00000357951.3:p.Val270Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.808G>A
  hgvsp: ENSP00000343175.3:p.Val270Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.808G>A
  hgvsp: ENSP00000342210.3:p.Val270Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.808G>A
  hgvsp: ENSP00000357952.2:p.Val270Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.808G>A
  hgvsp: ENSP00000327747.4:p.Val270Met
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1160G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.808G>A
  hgvsp: ENSP00000357905.3:p.Val270Met
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39589
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53041
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3079
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val270Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

10-124339224-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339224
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339224
    reference: chr 10
allele count: 1
allele frequency: 8.287063893262618e-6
allele num: 120670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1158G>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.810G>T
  hgvsp: ENST00000338354.3:c.810G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.810G>T
  hgvsp: ENST00000368955.3:c.810G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.810G>T
  hgvsp: ENST00000368909.3:c.810G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.810G>T
  hgvsp: ENST00000330163.4:c.810G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.810G>T
  hgvsp: ENST00000368956.2:c.810G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.810G>T
  hgvsp: ENST00000344338.3:c.810G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val270Val
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

10-124339225-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339225
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339225
    reference: chr 10
allele count: 1
allele frequency: 8.287888080359362e-6
allele num: 120658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.811G>A
  hgvsp: ENSP00000342210.3:p.Val271Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1157G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.811G>A
  hgvsp: ENSP00000357952.2:p.Val271Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.811G>A
  hgvsp: ENSP00000357905.3:p.Val271Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.811G>A
  hgvsp: ENSP00000357951.3:p.Val271Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.811G>A
  hgvsp: ENSP00000343175.3:p.Val271Ile
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.811G>A
  hgvsp: ENSP00000327747.4:p.Val271Ile
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val271Ile
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

10-124339236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339236
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339236
    reference: chr 10
allele count: 1
allele frequency: 8.29324929507381e-6
allele num: 120580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.822G>A
  hgvsp: ENST00000338354.3:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.822G>A
  hgvsp: ENST00000368955.3:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1146G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.822G>A
  hgvsp: ENST00000368956.2:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.822G>A
  hgvsp: ENST00000344338.3:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.822G>A
  hgvsp: ENST00000330163.4:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.822G>A
  hgvsp: ENST00000368909.3:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln274Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

10-124339249-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339249
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339249
    reference: chr 10
allele count: 3
allele frequency: 2.490081176646359e-5
allele num: 120478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.835T>G
  hgvsp: ENSP00000342210.3:p.Trp279Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.835T>G
  hgvsp: ENSP00000327747.4:p.Trp279Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.835T>G
  hgvsp: ENSP00000357952.2:p.Trp279Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.835T>G
  hgvsp: ENSP00000357905.3:p.Trp279Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.835T>G
  hgvsp: ENSP00000343175.3:p.Trp279Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.835T>G
  hgvsp: ENSP00000357951.3:p.Trp279Gly
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1133T>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39587
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53011
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Trp279Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

10-124339256-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339256
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339256
    reference: chr 10
allele count: 88
allele frequency: 7.304965716467717e-4
allele num: 120466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.842T>C
  hgvsp: ENSP00000357951.3:p.Met281Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1126T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.842T>C
  hgvsp: ENSP00000327747.4:p.Met281Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.842T>C
  hgvsp: ENSP00000357952.2:p.Met281Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.842T>C
  hgvsp: ENSP00000357905.3:p.Met281Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.842T>C
  hgvsp: ENSP00000342210.3:p.Met281Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.842T>C
  hgvsp: ENSP00000343175.3:p.Met281Thr
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39579
  bin: 9.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met281Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

10-124339260-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339260
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339260
    reference: chr 10
allele count: 5
allele frequency: 4.151651526977432e-5
allele num: 120434
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.846A>G
  hgvsp: ENST00000368956.2:c.846A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.846A>G
  hgvsp: ENST00000368955.3:c.846A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.846A>G
  hgvsp: ENST00000344338.3:c.846A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.846A>G
  hgvsp: ENST00000338354.3:c.846A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.846A>G
  hgvsp: ENST00000330163.4:c.846A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.846A>G
  hgvsp: ENST00000368909.3:c.846A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1122A>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39554
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser282Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

10-124339268-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339268
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339268
    reference: chr 10
allele count: 13
allele frequency: 1.079949491593009e-4
allele num: 120376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.854G>T
  hgvsp: ENSP00000327747.4:p.Gly285Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.854G>T
  hgvsp: ENSP00000357905.3:p.Gly285Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.854G>T
  hgvsp: ENSP00000342210.3:p.Gly285Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1114G>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.854G>T
  hgvsp: ENSP00000357951.3:p.Gly285Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.854G>T
  hgvsp: ENSP00000343175.3:p.Gly285Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.854G>T
  hgvsp: ENSP00000357952.2:p.Gly285Val
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39558
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2590
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly285Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

10-124339271-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339271
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339271
    reference: chr 10
allele count: 1
allele frequency: 8.306061763875276e-6
allele num: 120394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.857A>G
  hgvsp: ENSP00000357952.2:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.857A>G
  hgvsp: ENSP00000342210.3:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.857A>G
  hgvsp: ENSP00000357951.3:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1111A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.857A>G
  hgvsp: ENSP00000327747.4:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.857A>G
  hgvsp: ENSP00000357905.3:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.857A>G
  hgvsp: ENSP00000343175.3:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39550
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53062
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn286Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/10-124339274-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339274
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339274
    reference: chr 10
allele count: 18
allele frequency: 1.495463759928218e-4
allele num: 120364
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.860C>A
  hgvsp: ENSP00000357905.3:p.Ala287Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.860C>A
  hgvsp: ENSP00000343175.3:p.Ala287Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.860C>A
  hgvsp: ENSP00000342210.3:p.Ala287Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.860C>A
  hgvsp: ENSP00000357952.2:p.Ala287Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.860C>A
  hgvsp: ENSP00000327747.4:p.Ala287Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.860C>A
  hgvsp: ENSP00000357951.3:p.Ala287Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1108C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39550
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala287Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

10-124339275-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339275
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339275
    reference: chr 10
allele count: 2
allele frequency: 1.661792076575379e-5
allele num: 120352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1107C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.861C>G
  hgvsp: ENST00000330163.4:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.861C>G
  hgvsp: ENST00000344338.3:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.861C>G
  hgvsp: ENST00000368909.3:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.861C>G
  hgvsp: ENST00000368955.3:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.861C>G
  hgvsp: ENST00000338354.3:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.861C>G
  hgvsp: ENST00000368956.2:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39546
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53062
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala287Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/10-124339277-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339277
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339277
    reference: chr 10
allele count: 1
allele frequency: 8.309788931361144e-6
allele num: 120340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.863A>C
  hgvsp: ENSP00000357952.2:p.Gln288Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.863A>C
  hgvsp: ENSP00000327747.4:p.Gln288Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.863A>C
  hgvsp: ENSP00000342210.3:p.Gln288Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.863A>C
  hgvsp: ENSP00000357951.3:p.Gln288Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.863A>C
  hgvsp: ENSP00000343175.3:p.Gln288Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.863A>C
  hgvsp: ENSP00000357905.3:p.Gln288Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1105A>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39570
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53079
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2625
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln288Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-124339277-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339277
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339277
    reference: chr 10
allele count: 73
allele frequency: 6.066145919893635e-4
allele num: 120340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1105A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.863A>G
  hgvsp: ENSP00000343175.3:p.Gln288Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.863A>G
  hgvsp: ENSP00000327747.4:p.Gln288Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.863A>G
  hgvsp: ENSP00000342210.3:p.Gln288Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.863A>G
  hgvsp: ENSP00000357905.3:p.Gln288Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.863A>G
  hgvsp: ENSP00000357951.3:p.Gln288Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.863A>G
  hgvsp: ENSP00000357952.2:p.Gln288Arg
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39570
  bin: 9.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2625
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln288Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

10-124339280-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339280
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339280
    reference: chr 10
allele count: 1
allele frequency: 8.308546170591069e-6
allele num: 120358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.866T>A
  hgvsp: ENSP00000357951.3:p.Phe289Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.866T>A
  hgvsp: ENSP00000327747.4:p.Phe289Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.866T>A
  hgvsp: ENSP00000357952.2:p.Phe289Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.866T>A
  hgvsp: ENSP00000357905.3:p.Phe289Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1102T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.866T>A
  hgvsp: ENSP00000343175.3:p.Phe289Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.866T>A
  hgvsp: ENSP00000342210.3:p.Phe289Tyr
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2650
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe289Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

10-124339281-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339281
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339281
    reference: chr 10
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.867T>A
  hgvsp: ENSP00000343175.3:p.Phe289Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.867T>A
  hgvsp: ENSP00000327747.4:p.Phe289Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.867T>A
  hgvsp: ENSP00000357951.3:p.Phe289Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.867T>A
  hgvsp: ENSP00000342210.3:p.Phe289Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.867T>A
  hgvsp: ENSP00000357952.2:p.Phe289Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.867T>A
  hgvsp: ENSP00000357905.3:p.Phe289Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1101T>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe289Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

10-124339281-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339281
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339281
    reference: chr 10
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1101T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.867T>C
  hgvsp: ENST00000368909.3:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.867T>C
  hgvsp: ENST00000338354.3:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.867T>C
  hgvsp: ENST00000330163.4:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.867T>C
  hgvsp: ENST00000368956.2:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.867T>C
  hgvsp: ENST00000344338.3:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.867T>C
  hgvsp: ENST00000368955.3:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe289Phe
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-124339283-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339283
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339283
    reference: chr 10
allele count: 1
allele frequency: 8.308684236764266e-6
allele num: 120356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.869G>T
  hgvsp: ENSP00000357951.3:p.Gly290Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.869G>T
  hgvsp: ENSP00000357952.2:p.Gly290Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.869G>T
  hgvsp: ENSP00000343175.3:p.Gly290Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.869G>T
  hgvsp: ENSP00000342210.3:p.Gly290Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.869G>T
  hgvsp: ENSP00000357905.3:p.Gly290Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.869G>T
  hgvsp: ENSP00000327747.4:p.Gly290Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1099G>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly290Val
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-124339284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339284
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339284
    reference: chr 10
allele count: 1
allele frequency: 8.309788931361144e-6
allele num: 120340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.870C>T
  hgvsp: ENST00000368955.3:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.870C>T
  hgvsp: ENST00000338354.3:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.870C>T
  hgvsp: ENST00000330163.4:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.870C>T
  hgvsp: ENST00000368909.3:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.870C>T
  hgvsp: ENST00000368956.2:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.870C>T
  hgvsp: ENST00000344338.3:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1098C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly290Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

10-124339287-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339287
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339287
    reference: chr 10
allele count: 1
allele frequency: 8.310065150910783e-6
allele num: 120336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1095G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.873G>A
  hgvsp: ENST00000344338.3:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.873G>A
  hgvsp: ENST00000368956.2:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.873G>A
  hgvsp: ENST00000368909.3:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.873G>A
  hgvsp: ENST00000330163.4:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.873G>A
  hgvsp: ENST00000338354.3:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.873G>A
  hgvsp: ENST00000368955.3:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39541
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53081
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln291Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

10-124339289-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339289
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339289
    reference: chr 10
allele count: 5
allele frequency: 4.155585106382979e-5
allele num: 120320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.875G>T
  hgvsp: ENSP00000357952.2:p.Gly292Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.875G>T
  hgvsp: ENSP00000327747.4:p.Gly292Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1093G>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.875G>T
  hgvsp: ENSP00000343175.3:p.Gly292Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.875G>T
  hgvsp: ENSP00000357951.3:p.Gly292Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.875G>T
  hgvsp: ENSP00000357905.3:p.Gly292Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.875G>T
  hgvsp: ENSP00000342210.3:p.Gly292Val
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39541
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly292Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-124339290-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339290
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339290
    reference: chr 10
allele count: 1
allele frequency: 8.312966565248474e-6
allele num: 120294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.876C>A
  hgvsp: ENST00000368956.2:c.876C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.876C>A
  hgvsp: ENST00000330163.4:c.876C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.876C>A
  hgvsp: ENST00000344338.3:c.876C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.876C>A
  hgvsp: ENST00000338354.3:c.876C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.876C>A
  hgvsp: ENST00000368909.3:c.876C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.876C>A
  hgvsp: ENST00000368955.3:c.876C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1092C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39540
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly292Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

10-124339294-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339294
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339294
    reference: chr 10
allele count: 1
allele frequency: 8.313104778372627e-6
allele num: 120292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.880G>A
  hgvsp: ENSP00000357952.2:p.Gly294Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.880G>A
  hgvsp: ENSP00000343175.3:p.Gly294Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.880G>A
  hgvsp: ENSP00000327747.4:p.Gly294Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.880G>A
  hgvsp: ENSP00000342210.3:p.Gly294Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.880G>A
  hgvsp: ENSP00000357951.3:p.Gly294Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.880G>A
  hgvsp: ENSP00000357905.3:p.Gly294Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1088G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 39540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53078
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2510
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly294Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

10-124339296-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339296
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339296
    reference: chr 10
allele count: 2
allele frequency: 1.662786830728301e-5
allele num: 120280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.882A>G
  hgvsp: ENST00000368955.3:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.882A>G
  hgvsp: ENST00000330163.4:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.882A>G
  hgvsp: ENST00000368909.3:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.882A>G
  hgvsp: ENST00000338354.3:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1086A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.882A>G
  hgvsp: ENST00000368956.2:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.882A>G
  hgvsp: ENST00000344338.3:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39540
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53079
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly294Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/10-124339298-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339298
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339298
    reference: chr 10
allele count: 1
allele frequency: 8.314625426124552e-6
allele num: 120270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.884C>A
  hgvsp: ENSP00000357952.2:p.Pro295His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.884C>A
  hgvsp: ENSP00000327747.4:p.Pro295His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.884C>A
  hgvsp: ENSP00000342210.3:p.Pro295His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.884C>A
  hgvsp: ENSP00000343175.3:p.Pro295His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.884C>A
  hgvsp: ENSP00000357951.3:p.Pro295His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.884C>A
  hgvsp: ENSP00000357905.3:p.Pro295His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1084C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro295His
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

10-124339304-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339304
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339304
    reference: chr 10
allele count: 1
allele frequency: 8.317806760713336e-6
allele num: 120224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1078T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.890T>C
  hgvsp: ENSP00000357952.2:p.Val297Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.890T>C
  hgvsp: ENSP00000342210.3:p.Val297Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.890T>C
  hgvsp: ENSP00000327747.4:p.Val297Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.890T>C
  hgvsp: ENSP00000343175.3:p.Val297Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.890T>C
  hgvsp: ENSP00000357951.3:p.Val297Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.890T>C
  hgvsp: ENSP00000357905.3:p.Val297Ala
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val297Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

10-124339305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339305
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339305
    reference: chr 10
allele count: 2
allele frequency: 1.66347833319471e-5
allele num: 120230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.891C>T
  hgvsp: ENST00000368956.2:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1077C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.891C>T
  hgvsp: ENST00000330163.4:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.891C>T
  hgvsp: ENST00000344338.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.891C>T
  hgvsp: ENST00000338354.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.891C>T
  hgvsp: ENST00000368909.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.891C>T
  hgvsp: ENST00000368955.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39540
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val297Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-124339309-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124339309
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124339309
    reference: chr 10
allele count: 1
allele frequency: 8.321821480285606e-6
allele num: 120166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.895G>T
  hgvsp: ENSP00000327747.4:p.Asp299Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.608-1073G>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.895G>T
  hgvsp: ENSP00000357951.3:p.Asp299Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.895G>T
  hgvsp: ENSP00000342210.3:p.Asp299Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.895G>T
  hgvsp: ENSP00000343175.3:p.Asp299Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.895G>T
  hgvsp: ENSP00000357952.2:p.Asp299Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.895G>T
  hgvsp: ENSP00000357905.3:p.Asp299Tyr
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp299Tyr
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 824
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3386
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 624
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

South Asian
type: Population
allele count: 10
allele frequency: 6.077549532028686e-4
allele num: 16454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1299e1

DP
type: SiteQuality
SIO_000300: 6.595691e6

QD
type: SiteQuality
SIO_000300: 3.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e0

VQSLOD
type: SiteQuality
SIO_000300: -5.363e0

MQ
type: SiteQuality
SIO_000300: 5.146e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.383e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.877e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

GenotypeQuality
all individuals: 52659
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 371
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 624
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.31e0

MQ
type: SiteQuality
SIO_000300: 4.8e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.349e0

DP
type: SiteQuality
SIO_000300: 6.595093e6

FS
type: SiteQuality
SIO_000300: 9.645e0

VQSLOD
type: SiteQuality
SIO_000300: -6.712e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.839e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.331e0

QD
type: SiteQuality
SIO_000300: 1.616e1

GenotypeQuality
all individuals: 828
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 746
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 372
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.68e0

MQRankSum
type: SiteQuality
SIO_000300: 9.01e-1

MQ
type: SiteQuality
SIO_000300: 5.413e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.099e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.016e0

QD
type: SiteQuality
SIO_000300: 1.314e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 6.595423e6

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52660
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 828
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 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: 66740
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.012e1

QD
type: SiteQuality
SIO_000300: 1.099e1

DP
type: SiteQuality
SIO_000300: 6.594977e6

MQRankSum
type: SiteQuality
SIO_000300: -6.18e0

VQSLOD
type: SiteQuality
SIO_000300: -5.117e0

FS
type: SiteQuality
SIO_000300: 2.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

GenotypeQuality
all individuals: 622
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1287
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 745
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 368
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 52685
bin: 9.75e1
variant carriers: 58

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

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 56
allele frequency: 3.391472868217054e-3
allele num: 16512
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 6.600768e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.237e1

MQRankSum
type: SiteQuality
SIO_000300: -2.885e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.258e0

MQ
type: SiteQuality
SIO_000300: 5.068e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1289
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52682
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 622
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 3.060599877576005e-4
allele num: 9802
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

South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.85e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

QD
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SIO_000300: 1.515e1

DP
type: SiteQuality
SIO_000300: 6.59501e6

MQ
type: SiteQuality
SIO_000300: 5.537e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.624e1

ClippingRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.131e0

VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

African
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allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

ClippingRankSum
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FS
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SIO_000300: 1.168e0

VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
SIO_000300: 5.608e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.119e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e0

QD
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SIO_000300: 1.804e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 17

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

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

Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 3.060599877576005e-4
allele num: 9802
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 12
allele frequency: 1.798022175606832e-4
allele num: 66740
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

FS
type: SiteQuality
SIO_000300: 1.7214e1

MQRankSum
type: SiteQuality
SIO_000300: -1.365e1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 4.943e1

QD
type: SiteQuality
SIO_000300: 9.02e0

DP
type: SiteQuality
SIO_000300: 6.596293e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.571e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.605e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.47e-2

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.593063e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16512
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.43e-1

InbreedingCoeff
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SIO_000300: 2.2e-3

MQ
type: SiteQuality
SIO_000300: 5.605e1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.019991840065279e-4
allele num: 9804
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
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Other
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South Asian
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MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.051e1

ReadPosRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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South Asian
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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QD
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DP
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MQ
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 29
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allele num: 9804
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Other
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European (Non-Finnish)
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allele num: 66740
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East Asian
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European (Finnish)
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South Asian
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Latino
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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Other
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Latino
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African
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allele frequency: 1.223990208078335e-3
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European (Non-Finnish)
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allele frequency: 2.996703626011388e-5
allele num: 66740
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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MQ
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QD
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FS
type: SiteQuality
SIO_000300: 4.5793e1

BaseQRankSum
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SIO_000300: 7.69e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9804
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Latino
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allele frequency: 0.0e0
allele num: 11576
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
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Other
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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MQRankSum
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MQ
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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allele frequency: 2.2271714922049e-3
allele num: 898
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9804
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European (Non-Finnish)
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allele count: 62
allele frequency: 9.289781240635301e-4
allele num: 66740
num of homozygotes: 0

East Asian
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allele frequency: 4.637143519591931e-4
allele num: 8626
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 76
allele frequency: 1.149077713940127e-2
allele num: 6614
num of homozygotes: 0

FS
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MQRankSum
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ClippingRankSum
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
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African
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Latino
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DP
type: SiteQuality
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VQSLOD
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MQ
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SIO_000300: 5.382e1

MQRankSum
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ClippingRankSum
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SIO_000300: 3.49e-1

ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 2.446e0

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

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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QD
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SIO_000300: 1.342e1

FS
type: SiteQuality
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 1.7e-3

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e-1

MQ
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SIO_000300: 5.382e1

MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 11
allele frequency: 1.121991024071807e-3
allele num: 9804
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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DP
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
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East Asian
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allele frequency: 0.0e0
allele num: 8626
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African
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allele frequency: 0.0e0
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Other
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Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
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South Asian
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MQ
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DP
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66738
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European (Finnish)
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allele num: 6614
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Latino
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Other
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South Asian
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allele frequency: 7.873062015503876e-4
allele num: 16512
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African
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East Asian
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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QD
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InbreedingCoeff
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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Other
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European (Finnish)
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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DP
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6614
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East Asian
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African
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Latino
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Other
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South Asian
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European (Non-Finnish)
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allele num: 66738
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FS
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VQSLOD
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QD
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.638562543192813e-4
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Other
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African
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South Asian
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.018909766549792e-3
allele num: 66738
num of homozygotes: 0

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.498621268433042e-5
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Latino
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allele frequency: 0.0e0
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East Asian
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Other
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African
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allele frequency: 0.0e0
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South Asian
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allele num: 16512
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FS
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DP
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MQ
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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SIO_000300: 9.399999999999999e-1

ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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allele num: 8626
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele num: 16512
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Other
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allele frequency: 0.0e0
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MQ
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SIO_000300: 4.883e1

InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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FS
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QD
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BaseQRankSum
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SIO_000300: -5.039e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66724
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Latino
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Other
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num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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QD
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DP
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.638562543192813e-4
allele num: 11576
num of homozygotes: 0

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

African
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East Asian
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Other
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European (Non-Finnish)
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allele num: 66724
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South Asian
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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East Asian
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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East Asian
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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African
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South Asian
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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Latino
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 4.933e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.77e-1

DP
type: SiteQuality
SIO_000300: 6.593e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.385e1

MQ
type: SiteQuality
SIO_000300: 4.849e1

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

GenotypeQuality
all individuals: 602
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3264
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52815
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1241
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 810
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 12
allele frequency: 1.036627505183138e-3
allele num: 11576
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 6.593595e6

FS
type: SiteQuality
SIO_000300: 1.815e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e-2

QD
type: SiteQuality
SIO_000300: 2.09e0

MQRankSum
type: SiteQuality
SIO_000300: -2.938e0

VQSLOD
type: SiteQuality
SIO_000300: -5.668e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.607e0

MQ
type: SiteQuality
SIO_000300: 4.599e1

GenotypeQuality
all individuals: 462
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3160
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 589
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1220
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 3

African
type: Population
allele count: 4
allele frequency: 4.097520999795124e-4
allele num: 9762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
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: 3
allele frequency: 3.494060097833683e-4
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 60
allele frequency: 3.705075954057058e-3
allele num: 16194
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.463e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.650257e6

MQRankSum
type: SiteQuality
SIO_000300: -4.655e0

VQSLOD
type: SiteQuality
SIO_000300: -7.876e0

FS
type: SiteQuality
SIO_000300: 2.0884e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.562e0

QD
type: SiteQuality
SIO_000300: 3.6e-1

MQ
type: SiteQuality
SIO_000300: 4.383e1

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3146
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
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GenotypeQuality
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
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variant carriers: 0

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

GenotypeQuality
all individuals: 1210
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 319
allele frequency: 1.931928294573643e-2
allele num: 16512
num of homozygotes: 5

Latino
type: Population
allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.85e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.1e0

QD
type: SiteQuality
SIO_000300: 9.93e0

VQSLOD
type: SiteQuality
SIO_000300: -4.227e0

FS
type: SiteQuality
SIO_000300: 6.169e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.806e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

MQ
type: SiteQuality
SIO_000300: 4.302e1

DP
type: SiteQuality
SIO_000300: 6.600885e6

GenotypeQuality
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3150
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53052
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 52
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variant carriers: 0

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

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 353
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 1208
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 12
allele frequency: 1.036806635562468e-3
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.686e0

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

FS
type: SiteQuality
SIO_000300: 4.052e0

DP
type: SiteQuality
SIO_000300: 6.600921e6

MQ
type: SiteQuality
SIO_000300: 4.275e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.43e0

MQRankSum
type: SiteQuality
SIO_000300: -4.193e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.24e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
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variant carriers: 0

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

GenotypeQuality
all individuals: 53052
bin: 9.75e1
variant carriers: 317

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
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variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

South Asian
type: Population
allele count: 319
allele frequency: 1.931928294573643e-2
allele num: 16512
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

DP
type: SiteQuality
SIO_000300: 6.600921e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.24e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.43e0

FS
type: SiteQuality
SIO_000300: 4.052e0

MQRankSum
type: SiteQuality
SIO_000300: -4.193e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.686e0

MQ
type: SiteQuality
SIO_000300: 4.275e1

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

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3068
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

MQ
type: SiteQuality
SIO_000300: 4.172e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -2.224e0

FS
type: SiteQuality
SIO_000300: 6.07e-1

DP
type: SiteQuality
SIO_000300: 6.575165e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.008e0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.89e-1

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
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GenotypeQuality
all individuals: 53048
bin: 9.75e1
variant carriers: 13

GenotypeQuality
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GenotypeQuality
all individuals: 70
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GenotypeQuality
all individuals: 700
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GenotypeQuality
all individuals: 11
bin: 4.25e1
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GenotypeQuality
all individuals: 1188
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.25e1
variant carriers: 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: 9778
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.036806635562468e-3
allele num: 11574
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.408e1

VQSLOD
type: SiteQuality
SIO_000300: -9.903e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.74e0

DP
type: SiteQuality
SIO_000300: 6.575035e6

QD
type: SiteQuality
SIO_000300: 1.83e0

FS
type: SiteQuality
SIO_000300: 6.721e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.206e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.574e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 6
bin: 4.75e1
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GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53048
bin: 9.75e1
variant carriers: 1

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: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.022704029453876e-4
allele num: 9778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
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: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.83e0

MQRankSum
type: SiteQuality
SIO_000300: -3.243e0

FS
type: SiteQuality
SIO_000300: 6.02e-1

DP
type: SiteQuality
SIO_000300: 6.573246e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQ
type: SiteQuality
SIO_000300: 4.283e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.329e0

VQSLOD
type: SiteQuality
SIO_000300: -4.901e0

QD
type: SiteQuality
SIO_000300: 5.77e0

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

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 700
bin: 8.25e1
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GenotypeQuality
all individuals: 53048
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497751124437781e-5
allele num: 66700
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 4.418e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.558e0

FS
type: SiteQuality
SIO_000300: 1.821e0

VQSLOD
type: SiteQuality
SIO_000300: -2.475e0

DP
type: SiteQuality
SIO_000300: 6.573455e6

QD
type: SiteQuality
SIO_000300: 1.113e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.051e0

GenotypeQuality
all individuals: 700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
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GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53051
bin: 9.75e1
variant carriers: 224

GenotypeQuality
all individuals: 777
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 577
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 140
allele frequency: 2.099139352865325e-3
allele num: 66694
num of homozygotes: 1

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

African
type: Population
allele count: 3
allele frequency: 3.069367710251688e-4
allele num: 9774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 75
allele frequency: 1.133958270335652e-2
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.34075723830735e-3
allele num: 898
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.197e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -8.578e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

DP
type: SiteQuality
SIO_000300: 6.596286e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.378e0

MQ
type: SiteQuality
SIO_000300: 4.572e1

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

GenotypeQuality
all individuals: 3102
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 457
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 114
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

MQ
type: SiteQuality
SIO_000300: 3.889e1

MQRankSum
type: SiteQuality
SIO_000300: -9.074e0

FS
type: SiteQuality
SIO_000300: 1.47398e2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.68e0

DP
type: SiteQuality
SIO_000300: 6.556018e6

VQSLOD
type: SiteQuality
SIO_000300: -1.074e2

QD
type: SiteQuality
SIO_000300: 8.27e0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 777
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 457
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.555669e6

FS
type: SiteQuality
SIO_000300: 2.289e0

QD
type: SiteQuality
SIO_000300: 8.73e0

MQRankSum
type: SiteQuality
SIO_000300: -7.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.374e0

MQ
type: SiteQuality
SIO_000300: 4.157e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

GenotypeQuality
all individuals: 136
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3088
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53041
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.04e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

DP
type: SiteQuality
SIO_000300: 6.555735e6

FS
type: SiteQuality
SIO_000300: 6.24e-1

MQ
type: SiteQuality
SIO_000300: 4.427e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.986e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: -2.031e0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 53041
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 457
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

VQSLOD
type: SiteQuality
SIO_000300: -2.284e0

FS
type: SiteQuality
SIO_000300: 9.207000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.19e-1

MQ
type: SiteQuality
SIO_000300: 5.262e1

DP
type: SiteQuality
SIO_000300: 6.554907e6

QD
type: SiteQuality
SIO_000300: 3.34e0

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53040
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 457
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2889
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.551203e6

FS
type: SiteQuality
SIO_000300: 9.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 3.872e1

VQSLOD
type: SiteQuality
SIO_000300: -2.955e0

QD
type: SiteQuality
SIO_000300: 8.279999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

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

GenotypeQuality
all individuals: 1107
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2775
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variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
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variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.506940688660537e-5
allele num: 66564
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.8e-1

MQ
type: SiteQuality
SIO_000300: 4.249e1

DP
type: SiteQuality
SIO_000300: 6.549172e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -2.569e0

QD
type: SiteQuality
SIO_000300: 1.146e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 453
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GenotypeQuality
all individuals: 682
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53063
bin: 9.75e1
variant carriers: 88

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 34
allele frequency: 2.059108527131783e-3
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.012798173406237e-5
allele num: 66572
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: 46
allele frequency: 4.755996691480562e-3
allele num: 9672
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.361e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 3.832e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: -3.089e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.266e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.055e0

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

DP
type: SiteQuality
SIO_000300: 6.54526e6

GenotypeQuality
all individuals: 762
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 2.25e1
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GenotypeQuality
all individuals: 2637
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variant carriers: 0

GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 53056
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 1068
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GenotypeQuality
all individuals: 560
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variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.010157165609881e-5
allele num: 66554
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 8.077999999999999e0

QD
type: SiteQuality
SIO_000300: 1.0e1

DP
type: SiteQuality
SIO_000300: 6.536316e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.23e0

MQ
type: SiteQuality
SIO_000300: 3.888e1

MQRankSum
type: SiteQuality
SIO_000300: -1.552e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.45e-1

GenotypeQuality
all individuals: 53062
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 757
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variant carriers: 0

GenotypeQuality
all individuals: 1055
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9638
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

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.954416982380179e-4
allele num: 66516
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.793e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 1.893e0

VQSLOD
type: SiteQuality
SIO_000300: -2.755e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-2

DP
type: SiteQuality
SIO_000300: 6.535202e6

QD
type: SiteQuality
SIO_000300: 1.242e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.337e0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 395
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 757
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9638
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQRankSum
type: SiteQuality
SIO_000300: -2.306e0

FS
type: SiteQuality
SIO_000300: 6.901e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.84e0

MQ
type: SiteQuality
SIO_000300: 3.668e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.883e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.065e0

DP
type: SiteQuality
SIO_000300: 6.534377e6

QD
type: SiteQuality
SIO_000300: 1.272e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 1048
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53062
bin: 9.75e1
variant carriers: 18

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.255367775305226e-4
allele num: 66508
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.304e0

DP
type: SiteQuality
SIO_000300: 6.534249e6

QD
type: SiteQuality
SIO_000300: 1.176e1

MQ
type: SiteQuality
SIO_000300: 3.759e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

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

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 454
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variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007428348019608e-5
allele num: 66502
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: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

FS
type: SiteQuality
SIO_000300: 5.483e0

DP
type: SiteQuality
SIO_000300: 6.532708e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.06e-1

MQ
type: SiteQuality
SIO_000300: 3.901e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.031e0

QD
type: SiteQuality
SIO_000300: 1.281e1

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

GenotypeQuality
all individuals: 674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
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GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 450
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variant carriers: 0

GenotypeQuality
all individuals: 396
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variant carriers: 0

GenotypeQuality
all individuals: 559
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 350
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variant carriers: 0

GenotypeQuality
all individuals: 1040
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
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: 896
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: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.535592e6

MQ
type: SiteQuality
SIO_000300: 3.56e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.549e0

FS
type: SiteQuality
SIO_000300: 9.821999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -3.952e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 5.48e0

MQRankSum
type: SiteQuality
SIO_000300: -1.561e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

GenotypeQuality
all individuals: 53079
bin: 9.75e1
variant carriers: 73

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 450
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GenotypeQuality
all individuals: 1040
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66488
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: 73
allele frequency: 4.421027131782946e-3
allele num: 16512
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: 896
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.549e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

DP
type: SiteQuality
SIO_000300: 6.535592e6

QD
type: SiteQuality
SIO_000300: 5.48e0

VQSLOD
type: SiteQuality
SIO_000300: -3.952e0

FS
type: SiteQuality
SIO_000300: 9.821999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 3.56e1

MQRankSum
type: SiteQuality
SIO_000300: -1.561e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 53080
bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 1
allele frequency: 1.037129226301597e-4
allele num: 9642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 896
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 3.268e1

VQSLOD
type: SiteQuality
SIO_000300: -2.683e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.242e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 8.38e-1

DP
type: SiteQuality
SIO_000300: 6.532596e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.576e0

QD
type: SiteQuality
SIO_000300: 1.277e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9638
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

MQ
type: SiteQuality
SIO_000300: 3.704e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.14e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.785e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.532312e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.334e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 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
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num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.532312e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.704e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.14e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503804625703029e-5
allele num: 66498
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9636
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.142e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53080
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 896
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 6.531967e6

MQ
type: SiteQuality
SIO_000300: 3.533e1

QD
type: SiteQuality
SIO_000300: 1.301e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -6.734e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.913e0

FS
type: SiteQuality
SIO_000300: 2.2791e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9632
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: 8624
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: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504166541319455e-5
allele num: 66482
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.039e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.989e0

VQSLOD
type: SiteQuality
SIO_000300: -2.454e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

FS
type: SiteQuality
SIO_000300: 4.743e0

DP
type: SiteQuality
SIO_000300: 6.531421e6

MQ
type: SiteQuality
SIO_000300: 4.246e1

QD
type: SiteQuality
SIO_000300: 1.369e1

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.017933441656135e-5
allele num: 66468
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

FS
type: SiteQuality
SIO_000300: 2.898e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 3.415e1

DP
type: SiteQuality
SIO_000300: 6.531018e6

VQSLOD
type: SiteQuality
SIO_000300: -2.442e0

QD
type: SiteQuality
SIO_000300: 1.165e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.367e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 53080
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9618
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.193e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.52e-1

DP
type: SiteQuality
SIO_000300: 6.530475e6

VQSLOD
type: SiteQuality
SIO_000300: -2.513e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.121e1

MQ
type: SiteQuality
SIO_000300: 4.024e1

GenotypeQuality
all individuals: 482
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 553
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variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
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variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9620
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

DP
type: SiteQuality
SIO_000300: 6.529712e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.151e1

MQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.135e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.609e0

GenotypeQuality
all individuals: 486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 677
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 134
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variant carriers: 0

GenotypeQuality
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009691205682297e-5
allele num: 66452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 2.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.754e0

QD
type: SiteQuality
SIO_000300: 1.301e1

FS
type: SiteQuality
SIO_000300: 7.119e0

MQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

DP
type: SiteQuality
SIO_000300: 6.529555e6

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 2.851e1

VQSLOD
type: SiteQuality
SIO_000300: -4.349e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.509e0

FS
type: SiteQuality
SIO_000300: 3.329e0

MQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

DP
type: SiteQuality
SIO_000300: 6.529005e6

QD
type: SiteQuality
SIO_000300: 2.065e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66414
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.3789e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.74e0

VQSLOD
type: SiteQuality
SIO_000300: -5.35e0

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 5.71e0

DP
type: SiteQuality
SIO_000300: 6.527894e6

MQ
type: SiteQuality
SIO_000300: 2.999e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9598
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 66414
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.021e1

MQ
type: SiteQuality
SIO_000300: 2.931e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.009e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0