19-7809012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809012
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809012
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+815G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.286G>A
  hgvsp: ENSP00000377716.4:p.Gly96Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.511G>A
  hgvsp: ENSP00000377728.4:p.Gly171Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.784G>A
  hgvsp: ENSP00000470530.1:p.Gly262Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.862G>A
  hgvsp: ENSP00000204801.7:p.Gly288Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.586G>A
  hgvsp: ENSP00000471348.1:p.Gly196Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.994G>A
  hgvsp: ENSP00000315477.6:p.Gly332Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.922G>A
  hgvsp: ENSP00000468827.1:p.Gly308Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.586G>A
  hgvsp: ENSP00000301357.8:p.Gly196Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.976G>A
  hgvsp: ENSP00000346373.5:p.Gly326Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.718G>A
  hgvsp: ENSP00000471137.1:p.Gly240Ser
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.922G>A
  hgvsp: ENSP00000315407.7:p.Gly308Ser
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly332Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

19-7809013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809013
    reference: chr 19
allele count: 1034
allele frequency: 8.517157872193209e-3
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.975C>T
  hgvsp: ENST00000354397.6:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.921C>T
  hgvsp: ENST00000315591.8:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.510C>T
  hgvsp: ENST00000394173.4:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.861C>T
  hgvsp: ENST00000204801.8:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.921C>T
  hgvsp: ENST00000601951.1:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.585C>T
  hgvsp: ENST00000593821.1:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.783C>T
  hgvsp: ENST00000593660.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.285C>T
  hgvsp: ENST00000394161.5:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.993C>T
  hgvsp: ENST00000315599.7:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.585C>T
  hgvsp: ENST00000301357.8:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+814C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.717C>T
  hgvsp: ENST00000602261.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 18548
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14594
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 9.75e1
  variant carriers: 394
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
hgvs: p.Asp331Asp
num of homozygotes: 6
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

19-7809015-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809015
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.781G>C
  hgvsp: ENSP00000470530.1:p.Asp261His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.919G>C
  hgvsp: ENSP00000468827.1:p.Asp307His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.919G>C
  hgvsp: ENSP00000315407.7:p.Asp307His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.859G>C
  hgvsp: ENSP00000204801.7:p.Asp287His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.973G>C
  hgvsp: ENSP00000346373.5:p.Asp325His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.508G>C
  hgvsp: ENSP00000377728.4:p.Asp170His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.283G>C
  hgvsp: ENSP00000377716.4:p.Asp95His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.583G>C
  hgvsp: ENSP00000301357.8:p.Asp195His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.715G>C
  hgvsp: ENSP00000471137.1:p.Asp239His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.991G>C
  hgvsp: ENSP00000315477.6:p.Asp331His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.583G>C
  hgvsp: ENSP00000471348.1:p.Asp195His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+812G>C
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp331His
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

19-7809025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809025
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809025
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.273G>A
  hgvsp: ENSP00000377716.4:p.Trp91Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.573G>A
  hgvsp: ENSP00000471348.1:p.Trp191Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+802G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.909G>A
  hgvsp: ENSP00000315407.7:p.Trp303Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.849G>A
  hgvsp: ENSP00000204801.7:p.Trp283Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.498G>A
  hgvsp: ENSP00000377728.4:p.Trp166Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.705G>A
  hgvsp: ENSP00000471137.1:p.Trp235Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.573G>A
  hgvsp: ENSP00000301357.8:p.Trp191Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.981G>A
  hgvsp: ENSP00000315477.6:p.Trp327Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.909G>A
  hgvsp: ENSP00000468827.1:p.Trp303Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.963G>A
  hgvsp: ENSP00000346373.5:p.Trp321Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.771G>A
  hgvsp: ENSP00000470530.1:p.Trp257Ter
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11935
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp327Ter
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

19-7809028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809028
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809028
    reference: chr 19
allele count: 11
allele frequency: 9.060209208467177e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.906G>A
  hgvsp: ENST00000315591.8:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.495G>A
  hgvsp: ENST00000394173.4:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.570G>A
  hgvsp: ENST00000301357.8:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.570G>A
  hgvsp: ENST00000593821.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.270G>A
  hgvsp: ENST00000394161.5:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.978G>A
  hgvsp: ENST00000315599.7:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.768G>A
  hgvsp: ENST00000593660.1:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.702G>A
  hgvsp: ENST00000602261.1:c.702G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+799G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.846G>A
  hgvsp: ENST00000204801.8:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.960G>A
  hgvsp: ENST00000354397.6:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.906G>A
  hgvsp: ENST00000601951.1:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11935
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr326Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

19-7809029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809029
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809029
    reference: chr 19
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.569C>T
  hgvsp: ENSP00000301357.8:p.Thr190Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+798C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.959C>T
  hgvsp: ENSP00000346373.5:p.Thr320Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.905C>T
  hgvsp: ENSP00000468827.1:p.Thr302Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.701C>T
  hgvsp: ENSP00000471137.1:p.Thr234Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.494C>T
  hgvsp: ENSP00000377728.4:p.Thr165Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.845C>T
  hgvsp: ENSP00000204801.7:p.Thr282Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.767C>T
  hgvsp: ENSP00000470530.1:p.Thr256Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.977C>T
  hgvsp: ENSP00000315477.6:p.Thr326Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.569C>T
  hgvsp: ENSP00000471348.1:p.Thr190Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.269C>T
  hgvsp: ENSP00000377716.4:p.Thr90Met
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.905C>T
  hgvsp: ENSP00000315407.7:p.Thr302Met
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr326Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

19-7809029-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809029
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809029
    reference: chr 19
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.494C>A
  hgvsp: ENSP00000377728.4:p.Thr165Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.905C>A
  hgvsp: ENSP00000468827.1:p.Thr302Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.569C>A
  hgvsp: ENSP00000301357.8:p.Thr190Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.845C>A
  hgvsp: ENSP00000204801.7:p.Thr282Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.767C>A
  hgvsp: ENSP00000470530.1:p.Thr256Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.959C>A
  hgvsp: ENSP00000346373.5:p.Thr320Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.701C>A
  hgvsp: ENSP00000471137.1:p.Thr234Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.977C>A
  hgvsp: ENSP00000315477.6:p.Thr326Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.905C>A
  hgvsp: ENSP00000315407.7:p.Thr302Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.569C>A
  hgvsp: ENSP00000471348.1:p.Thr190Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.269C>A
  hgvsp: ENSP00000377716.4:p.Thr90Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+798C>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr326Lys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-7809032-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809032
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809032
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.974G>C
  hgvsp: ENSP00000315477.6:p.Gly325Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.698G>C
  hgvsp: ENSP00000471137.1:p.Gly233Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.764G>C
  hgvsp: ENSP00000470530.1:p.Gly255Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+795G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.566G>C
  hgvsp: ENSP00000471348.1:p.Gly189Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.902G>C
  hgvsp: ENSP00000315407.7:p.Gly301Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.566G>C
  hgvsp: ENSP00000301357.8:p.Gly189Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.842G>C
  hgvsp: ENSP00000204801.7:p.Gly281Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.266G>C
  hgvsp: ENSP00000377716.4:p.Gly89Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.956G>C
  hgvsp: ENSP00000346373.5:p.Gly319Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.491G>C
  hgvsp: ENSP00000377728.4:p.Gly164Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.902G>C
  hgvsp: ENSP00000468827.1:p.Gly301Ala
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14651
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly325Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/19-7809051-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809051
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809051
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+776T>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.823T>G
  hgvsp: ENSP00000204801.7:p.Ser275Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.937T>G
  hgvsp: ENSP00000346373.5:p.Ser313Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.679T>G
  hgvsp: ENSP00000471137.1:p.Ser227Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.472T>G
  hgvsp: ENSP00000377728.4:p.Ser158Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.745T>G
  hgvsp: ENSP00000470530.1:p.Ser249Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.547T>G
  hgvsp: ENSP00000471348.1:p.Ser183Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.247T>G
  hgvsp: ENSP00000377716.4:p.Ser83Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.547T>G
  hgvsp: ENSP00000301357.8:p.Ser183Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.883T>G
  hgvsp: ENSP00000315407.7:p.Ser295Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.955T>G
  hgvsp: ENSP00000315477.6:p.Ser319Ala
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.883T>G
  hgvsp: ENSP00000468827.1:p.Ser295Ala
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser319Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

19-7809054-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809054
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809054
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.952C>T
  hgvsp: ENSP00000315477.6:p.Leu318Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.544C>T
  hgvsp: ENSP00000301357.8:p.Leu182Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.469C>T
  hgvsp: ENSP00000377728.4:p.Leu157Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.934C>T
  hgvsp: ENSP00000346373.5:p.Leu312Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.544C>T
  hgvsp: ENSP00000471348.1:p.Leu182Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+773C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.244C>T
  hgvsp: ENSP00000377716.4:p.Leu82Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.880C>T
  hgvsp: ENSP00000315407.7:p.Leu294Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.880C>T
  hgvsp: ENSP00000468827.1:p.Leu294Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.742C>T
  hgvsp: ENSP00000470530.1:p.Leu248Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.820C>T
  hgvsp: ENSP00000204801.7:p.Leu274Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.676C>T
  hgvsp: ENSP00000471137.1:p.Leu226Phe
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu318Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

19-7809056-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809056
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809056
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.674G>A
  hgvsp: ENSP00000471137.1:p.Gly225Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.878G>A
  hgvsp: ENSP00000468827.1:p.Gly293Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.878G>A
  hgvsp: ENSP00000315407.7:p.Gly293Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.542G>A
  hgvsp: ENSP00000471348.1:p.Gly181Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.242G>A
  hgvsp: ENSP00000377716.4:p.Gly81Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+771G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.740G>A
  hgvsp: ENSP00000470530.1:p.Gly247Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.950G>A
  hgvsp: ENSP00000315477.6:p.Gly317Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.818G>A
  hgvsp: ENSP00000204801.7:p.Gly273Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.932G>A
  hgvsp: ENSP00000346373.5:p.Gly311Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.542G>A
  hgvsp: ENSP00000301357.8:p.Gly181Glu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.467G>A
  hgvsp: ENSP00000377728.4:p.Gly156Glu
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly317Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

19-7809065-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809065
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809065
    reference: chr 19
allele count: 8
allele frequency: 6.589134517181169e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.533C>T
  hgvsp: ENSP00000301357.8:p.Thr178Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.665C>T
  hgvsp: ENSP00000471137.1:p.Thr222Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+762C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.869C>T
  hgvsp: ENSP00000468827.1:p.Thr290Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.923C>T
  hgvsp: ENSP00000346373.5:p.Thr308Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.533C>T
  hgvsp: ENSP00000471348.1:p.Thr178Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.809C>T
  hgvsp: ENSP00000204801.7:p.Thr270Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.941C>T
  hgvsp: ENSP00000315477.6:p.Thr314Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.869C>T
  hgvsp: ENSP00000315407.7:p.Thr290Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.458C>T
  hgvsp: ENSP00000377728.4:p.Thr153Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.731C>T
  hgvsp: ENSP00000470530.1:p.Thr244Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.233C>T
  hgvsp: ENSP00000377716.4:p.Thr78Ile
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr314Ile
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

19-7809070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809070
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809070
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.228C>T
  hgvsp: ENST00000394161.5:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.453C>T
  hgvsp: ENST00000394173.4:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.528C>T
  hgvsp: ENST00000593821.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.936C>T
  hgvsp: ENST00000315599.7:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.918C>T
  hgvsp: ENST00000354397.6:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+757C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.726C>T
  hgvsp: ENST00000593660.1:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.804C>T
  hgvsp: ENST00000204801.8:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.528C>T
  hgvsp: ENST00000301357.8:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.660C>T
  hgvsp: ENST00000602261.1:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.864C>T
  hgvsp: ENST00000315591.8:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.864C>T
  hgvsp: ENST00000601951.1:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg312Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/19-7809071-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809071
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809071
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.917G>T
  hgvsp: ENSP00000346373.5:p.Arg306Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+756G>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.935G>T
  hgvsp: ENSP00000315477.6:p.Arg312Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.227G>T
  hgvsp: ENSP00000377716.4:p.Arg76Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.527G>T
  hgvsp: ENSP00000471348.1:p.Arg176Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.863G>T
  hgvsp: ENSP00000315407.7:p.Arg288Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.803G>T
  hgvsp: ENSP00000204801.7:p.Arg268Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.725G>T
  hgvsp: ENSP00000470530.1:p.Arg242Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.659G>T
  hgvsp: ENSP00000471137.1:p.Arg220Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.863G>T
  hgvsp: ENSP00000468827.1:p.Arg288Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.452G>T
  hgvsp: ENSP00000377728.4:p.Arg151Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.527G>T
  hgvsp: ENSP00000301357.8:p.Arg176Leu
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14607
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg312Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

19-7809071-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809071
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809071
    reference: chr 19
allele count: 50
allele frequency: 4.11820907323823e-4
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.863G>A
  hgvsp: ENSP00000315407.7:p.Arg288His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.725G>A
  hgvsp: ENSP00000470530.1:p.Arg242His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.527G>A
  hgvsp: ENSP00000471348.1:p.Arg176His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.659G>A
  hgvsp: ENSP00000471137.1:p.Arg220His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.935G>A
  hgvsp: ENSP00000315477.6:p.Arg312His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.863G>A
  hgvsp: ENSP00000468827.1:p.Arg288His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.803G>A
  hgvsp: ENSP00000204801.7:p.Arg268His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.527G>A
  hgvsp: ENSP00000301357.8:p.Arg176His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.227G>A
  hgvsp: ENSP00000377716.4:p.Arg76His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.452G>A
  hgvsp: ENSP00000377728.4:p.Arg151His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.917G>A
  hgvsp: ENSP00000346373.5:p.Arg306His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+756G>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg312His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-7809072-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809072
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809072
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+755C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.934C>T
  hgvsp: ENSP00000315477.6:p.Arg312Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.862C>T
  hgvsp: ENSP00000468827.1:p.Arg288Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.862C>T
  hgvsp: ENSP00000315407.7:p.Arg288Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.658C>T
  hgvsp: ENSP00000471137.1:p.Arg220Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.724C>T
  hgvsp: ENSP00000470530.1:p.Arg242Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.226C>T
  hgvsp: ENSP00000377716.4:p.Arg76Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.916C>T
  hgvsp: ENSP00000346373.5:p.Arg306Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.526C>T
  hgvsp: ENSP00000301357.8:p.Arg176Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.526C>T
  hgvsp: ENSP00000471348.1:p.Arg176Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.802C>T
  hgvsp: ENSP00000204801.7:p.Arg268Cys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.451C>T
  hgvsp: ENSP00000377728.4:p.Arg151Cys
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg312Cys
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

19-7809073-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809073
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809073
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.450C>G
  hgvsp: ENSP00000377728.4:p.Asn150Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.861C>G
  hgvsp: ENSP00000468827.1:p.Asn287Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.525C>G
  hgvsp: ENSP00000301357.8:p.Asn175Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.525C>G
  hgvsp: ENSP00000471348.1:p.Asn175Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.225C>G
  hgvsp: ENSP00000377716.4:p.Asn75Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.801C>G
  hgvsp: ENSP00000204801.7:p.Asn267Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.723C>G
  hgvsp: ENSP00000470530.1:p.Asn241Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.933C>G
  hgvsp: ENSP00000315477.6:p.Asn311Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.657C>G
  hgvsp: ENSP00000471137.1:p.Asn219Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.915C>G
  hgvsp: ENSP00000346373.5:p.Asn305Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.861C>G
  hgvsp: ENSP00000315407.7:p.Asn287Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+754C>G
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn311Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

19-7809073-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809073
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809073
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.861C>A
  hgvsp: ENSP00000468827.1:p.Asn287Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.801C>A
  hgvsp: ENSP00000204801.7:p.Asn267Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.861C>A
  hgvsp: ENSP00000315407.7:p.Asn287Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.225C>A
  hgvsp: ENSP00000377716.4:p.Asn75Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.450C>A
  hgvsp: ENSP00000377728.4:p.Asn150Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.915C>A
  hgvsp: ENSP00000346373.5:p.Asn305Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.525C>A
  hgvsp: ENSP00000301357.8:p.Asn175Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.723C>A
  hgvsp: ENSP00000470530.1:p.Asn241Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+754C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.657C>A
  hgvsp: ENSP00000471137.1:p.Asn219Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.525C>A
  hgvsp: ENSP00000471348.1:p.Asn175Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.933C>A
  hgvsp: ENSP00000315477.6:p.Asn311Lys
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn311Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS

19-7809079-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809079
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809079
    reference: chr 19
allele count: 1669
allele frequency: 1.374748772692827e-2
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.855A>G
  hgvsp: ENST00000315591.8:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.909A>G
  hgvsp: ENST00000354397.6:c.909A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.519A>G
  hgvsp: ENST00000593821.1:c.519A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.855A>G
  hgvsp: ENST00000601951.1:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.519A>G
  hgvsp: ENST00000301357.8:c.519A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.717A>G
  hgvsp: ENST00000593660.1:c.717A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.927A>G
  hgvsp: ENST00000315599.7:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.444A>G
  hgvsp: ENST00000394173.4:c.444A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.795A>G
  hgvsp: ENST00000204801.8:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219A>G
  hgvsp: ENST00000394161.5:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+748A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.651A>G
  hgvsp: ENST00000602261.1:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 11676
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 9.75e1
  variant carriers: 942
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 18560
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 65
genotype quality: GenotypeQuality
hgvs: c.219A>G
num of homozygotes: 75
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-7809081-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809081
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809081
    reference: chr 19
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-2A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.517A>G
  hgvsp: ENSP00000471348.1:p.Arg173Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.715A>G
  hgvsp: ENSP00000470530.1:p.Arg239Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.649A>G
  hgvsp: ENSP00000471137.1:p.Arg217Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.907A>G
  hgvsp: ENSP00000346373.5:p.Arg303Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.853A>G
  hgvsp: ENSP00000315407.7:p.Arg285Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.853A>G
  hgvsp: ENSP00000468827.1:p.Arg285Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.793A>G
  hgvsp: ENSP00000204801.7:p.Arg265Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+746A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.442A>G
  hgvsp: ENSP00000377728.4:p.Arg148Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.517A>G
  hgvsp: ENSP00000301357.8:p.Arg173Gly
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.925A>G
  hgvsp: ENSP00000315477.6:p.Arg309Gly
  variant of: http://identifiers.org/hgnc/1641
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.219-2A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum

19-7809087-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809087
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809087
    reference: chr 19
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.919T>A
  hgvsp: ENSP00000315477.6:p.Ser307Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.787T>A
  hgvsp: ENSP00000204801.7:p.Ser263Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-8T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.511T>A
  hgvsp: ENSP00000301357.8:p.Ser171Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.511T>A
  hgvsp: ENSP00000471348.1:p.Ser171Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.847T>A
  hgvsp: ENSP00000468827.1:p.Ser283Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+740T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.436T>A
  hgvsp: ENSP00000377728.4:p.Ser146Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.847T>A
  hgvsp: ENSP00000315407.7:p.Ser283Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901T>A
  hgvsp: ENSP00000346373.5:p.Ser301Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.709T>A
  hgvsp: ENSP00000470530.1:p.Ser237Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.643T>A
  hgvsp: ENSP00000471137.1:p.Ser215Thr
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser307Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-7809088-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809088
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809088
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.510G>T
  hgvsp: ENSP00000471348.1:p.Gln170His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.918G>T
  hgvsp: ENSP00000315477.6:p.Gln306His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.435G>T
  hgvsp: ENSP00000377728.4:p.Gln145His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.786G>T
  hgvsp: ENSP00000204801.7:p.Gln262His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+739G>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.846G>T
  hgvsp: ENSP00000468827.1:p.Gln282His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.708G>T
  hgvsp: ENSP00000470530.1:p.Gln236His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-1G>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.642G>T
  hgvsp: ENSP00000471137.1:p.Gln214His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.846G>T
  hgvsp: ENSP00000315407.7:p.Gln282His
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-9G>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.510G>T
  hgvsp: ENSP00000301357.8:p.Gln170His
  variant of: http://identifiers.org/hgnc/1641
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11709
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.901-1G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

19-7809090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809090
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809090
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.844C>T
  hgvsp: ENSP00000315407.7:p.Gln282Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.706C>T
  hgvsp: ENSP00000470530.1:p.Gln236Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+737C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.916C>T
  hgvsp: ENSP00000315477.6:p.Gln306Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-11C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.640C>T
  hgvsp: ENSP00000471137.1:p.Gln214Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.844C>T
  hgvsp: ENSP00000468827.1:p.Gln282Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.433C>T
  hgvsp: ENSP00000377728.4:p.Gln145Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.508C>T
  hgvsp: ENSP00000471348.1:p.Gln170Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.784C>T
  hgvsp: ENSP00000204801.7:p.Gln262Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.508C>T
  hgvsp: ENSP00000301357.8:p.Gln170Ter
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln306Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

19-7809108-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809108
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809108
    reference: chr 19
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-21C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-29C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+719C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-3C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-3C>T
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.901-3C>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

19-7809111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809111
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809111
    reference: chr 19
allele count: 8
allele frequency: 6.597285217133149e-5
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-24C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-32C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-6C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+716C>T
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.901-6C>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

19-7809115-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809115
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809115
    reference: chr 19
allele count: 2
allele frequency: 1.649919978881024e-5
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-10T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-10T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-10T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-36T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-28T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+712T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-10T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-10T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-10T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-10T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-10T>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-10T>C
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-7809116-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809116
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809116
    reference: chr 19
allele count: 1670
allele frequency: 1.379207822668561e-2
allele num: 121084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+711G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-29G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-11G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-37G>C
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18354
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.75e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 3.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 5.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 4.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 11714
  bin: 3.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 13132
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
num of homozygotes: 75
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

19-7809128-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809128
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809128
    reference: chr 19
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-23C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-23C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-41C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-23C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-23C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-49C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-23C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-23C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-23C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-23C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+699C>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-23C>G
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

19-7809130-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809130
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809130
    reference: chr 19
allele count: 1
allele frequency: 8.270477702792114e-6
allele num: 120912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-51T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+697T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-25T>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-43T>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-7809140-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809140
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809140
    reference: chr 19
allele count: 1
allele frequency: 8.28775070445881e-6
allele num: 120660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-35C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-35C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-35C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-35C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-35C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-61C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-53C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-35C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+687C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-35C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-35C>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-35C>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11277
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

19-7809144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809144
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809144
    reference: chr 19
allele count: 4
allele frequency: 3.318455590768056e-5
allele num: 120538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-39G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-39G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-65G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-39G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-39G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-57G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-39G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-39G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-39G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+683G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-39G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-39G>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10483
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16285
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

19-7809145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809145
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809145
    reference: chr 19
allele count: 7
allele frequency: 5.809128630705394e-5
allele num: 120500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-58G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+682G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-40G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-66G>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11037
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-7809146-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809146
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809146
    reference: chr 19
allele count: 1
allele frequency: 8.304544246611745e-6
allele num: 120416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-59G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+681G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-41G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-67G>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10386
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

19-7809151-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809151
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809151
    reference: chr 19
allele count: 1
allele frequency: 8.316838270762986e-6
allele num: 120238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-46A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-46A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-46A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-46A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-46A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-64A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-46A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+676A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-72A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-46A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-46A>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-46A>T
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

19-7809156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809156
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809156
    reference: chr 19
allele count: 1
allele frequency: 8.348081610845828e-6
allele num: 119788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.493-51C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-77C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.901-69C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.769-51C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+671C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.829-51C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.829-51C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.691-51C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.418-51C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.625-51C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.901-51C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.493-51C>T
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10161
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

19-7809778-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809778
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809778
    reference: chr 19
allele count: 1
allele frequency: 8.342649291709075e-6
allele num: 119866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.492+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.492+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.624+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.900+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-699C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.768+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.417+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.690+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.900+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.828+49C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.828+49C>T
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

19-7809786-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809786
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809786
    reference: chr 19
allele count: 6
allele frequency: 4.999833338888704e-5
allele num: 120004
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.900+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.690+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-707C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.417+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.900+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.492+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.768+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.624+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.492+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.828+41C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.828+41C>T
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8358
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8692
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

19-7809793-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809793
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809793
    reference: chr 19
allele count: 4
allele frequency: 3.329837004478631e-5
allele num: 120126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.492+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.690+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.417+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.828+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.768+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.900+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.492+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-714G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.900+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.624+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+34G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.828+34G>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8174
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

19-7809795-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809795
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809795
    reference: chr 19
allele count: 2
allele frequency: 1.663838141825563e-5
allele num: 120204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.690+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.828+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.624+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.768+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.417+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.900+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.492+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-716A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.900+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.492+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.828+32A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+32A>G
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

19-7809797-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809797
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809797
    reference: chr 19
allele count: 1
allele frequency: 8.318637074501714e-6
allele num: 120212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.900+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.624+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-718C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.417+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.900+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.828+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.690+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.492+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.828+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.768+30C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.492+30C>T
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

19-7809805-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809805
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809805
    reference: chr 19
allele count: 159
allele frequency: 1.319918314489217e-3
allele num: 120462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.690+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-726G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.900+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.768+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.828+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.492+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.492+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.624+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.417+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.900+22G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.828+22G>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8361
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8294
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD

19-7809822-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809822
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809822
    reference: chr 19
allele count: 130
allele frequency: 1.073776720520699e-3
allele num: 121068
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.900+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.828+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.492+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.828+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.900+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.624+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-743A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.690+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.492+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.768+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.417+5A>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.828+5A>C
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8412
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 5.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: c.900+5A>C
num of homozygotes: 2
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

19-7809832-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809832
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809832
    reference: chr 19
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.823G>A
  hgvsp: ENSP00000470658.1:p.Glu275Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.685G>A
  hgvsp: ENSP00000470530.1:p.Glu229Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.619G>A
  hgvsp: ENSP00000471137.1:p.Glu207Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.895G>A
  hgvsp: ENSP00000346373.5:p.Glu299Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.823G>A
  hgvsp: ENSP00000468827.1:p.Glu275Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.823G>A
  hgvsp: ENSP00000315407.7:p.Glu275Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.895G>A
  hgvsp: ENSP00000315477.6:p.Glu299Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-753G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.763G>A
  hgvsp: ENSP00000204801.7:p.Glu255Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.487G>A
  hgvsp: ENSP00000471348.1:p.Glu163Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.487G>A
  hgvsp: ENSP00000301357.8:p.Glu163Lys
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.412G>A
  hgvsp: ENSP00000377728.4:p.Glu138Lys
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu299Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

19-7809835-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809835
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809835
    reference: chr 19
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.820G>C
  hgvsp: ENSP00000470658.1:p.Glu274Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.760G>C
  hgvsp: ENSP00000204801.7:p.Glu254Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.616G>C
  hgvsp: ENSP00000471137.1:p.Glu206Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.892G>C
  hgvsp: ENSP00000346373.5:p.Glu298Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.892G>C
  hgvsp: ENSP00000315477.6:p.Glu298Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.484G>C
  hgvsp: ENSP00000471348.1:p.Glu162Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.682G>C
  hgvsp: ENSP00000470530.1:p.Glu228Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-756G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.820G>C
  hgvsp: ENSP00000315407.7:p.Glu274Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.820G>C
  hgvsp: ENSP00000468827.1:p.Glu274Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.484G>C
  hgvsp: ENSP00000301357.8:p.Glu162Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.409G>C
  hgvsp: ENSP00000377728.4:p.Glu137Gln
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu298Gln
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

19-7809840-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809840
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809840
    reference: chr 19
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.611G>C
  hgvsp: ENSP00000471137.1:p.Ser204Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.815G>C
  hgvsp: ENSP00000315407.7:p.Ser272Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.404G>C
  hgvsp: ENSP00000377728.4:p.Ser135Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-761G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.815G>C
  hgvsp: ENSP00000470658.1:p.Ser272Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.479G>C
  hgvsp: ENSP00000471348.1:p.Ser160Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.479G>C
  hgvsp: ENSP00000301357.8:p.Ser160Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.677G>C
  hgvsp: ENSP00000470530.1:p.Ser226Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.755G>C
  hgvsp: ENSP00000204801.7:p.Ser252Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.887G>C
  hgvsp: ENSP00000315477.6:p.Ser296Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.887G>C
  hgvsp: ENSP00000346373.5:p.Ser296Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.815G>C
  hgvsp: ENSP00000468827.1:p.Ser272Thr
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser296Thr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-7809842-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809842
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809842
    reference: chr 19
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.675A>G
  hgvsp: ENST00000593660.1:c.675A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-763A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.753A>G
  hgvsp: ENST00000204801.8:c.753A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.885A>G
  hgvsp: ENST00000354397.6:c.885A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.813A>G
  hgvsp: ENST00000601256.1:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.885A>G
  hgvsp: ENST00000315599.7:c.885A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.402A>G
  hgvsp: ENST00000394173.4:c.402A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.477A>G
  hgvsp: ENST00000301357.8:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.813A>G
  hgvsp: ENST00000315591.8:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.477A>G
  hgvsp: ENST00000593821.1:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.609A>G
  hgvsp: ENST00000602261.1:c.609A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.813A>G
  hgvsp: ENST00000601951.1:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys295Lys
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-7809845-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809845
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809845
    reference: chr 19
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.474C>A
  hgvsp: ENST00000301357.8:c.474C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.750C>A
  hgvsp: ENST00000204801.8:c.750C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.810C>A
  hgvsp: ENST00000601256.1:c.810C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.672C>A
  hgvsp: ENST00000593660.1:c.672C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.474C>A
  hgvsp: ENST00000593821.1:c.474C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.882C>A
  hgvsp: ENST00000315599.7:c.882C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.882C>A
  hgvsp: ENST00000354397.6:c.882C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.810C>A
  hgvsp: ENST00000315591.8:c.810C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.810C>A
  hgvsp: ENST00000601951.1:c.810C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.606C>A
  hgvsp: ENST00000602261.1:c.606C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.399C>A
  hgvsp: ENST00000394173.4:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-766C>A
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile294Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

19-7809850-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809850
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809850
    reference: chr 19
allele count: 23
allele frequency: 1.895062949047525e-4
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.805G>C
  hgvsp: ENSP00000468827.1:p.Val269Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.877G>C
  hgvsp: ENSP00000315477.6:p.Val293Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.877G>C
  hgvsp: ENSP00000346373.5:p.Val293Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.745G>C
  hgvsp: ENSP00000204801.7:p.Val249Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.394G>C
  hgvsp: ENSP00000377728.4:p.Val132Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.667G>C
  hgvsp: ENSP00000470530.1:p.Val223Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-771G>C
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.805G>C
  hgvsp: ENSP00000470658.1:p.Val269Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.805G>C
  hgvsp: ENSP00000315407.7:p.Val269Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.469G>C
  hgvsp: ENSP00000471348.1:p.Val157Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.469G>C
  hgvsp: ENSP00000301357.8:p.Val157Leu
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.601G>C
  hgvsp: ENSP00000471137.1:p.Val201Leu
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val293Leu
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: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

19-7809850-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809850
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809850
    reference: chr 19
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.469G>A
  hgvsp: ENSP00000471348.1:p.Val157Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.805G>A
  hgvsp: ENSP00000315407.7:p.Val269Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.667G>A
  hgvsp: ENSP00000470530.1:p.Val223Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-771G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.877G>A
  hgvsp: ENSP00000346373.5:p.Val293Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.394G>A
  hgvsp: ENSP00000377728.4:p.Val132Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.877G>A
  hgvsp: ENSP00000315477.6:p.Val293Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.601G>A
  hgvsp: ENSP00000471137.1:p.Val201Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.469G>A
  hgvsp: ENSP00000301357.8:p.Val157Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.745G>A
  hgvsp: ENSP00000204801.7:p.Val249Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.805G>A
  hgvsp: ENSP00000470658.1:p.Val269Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.805G>A
  hgvsp: ENSP00000468827.1:p.Val269Ile
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val293Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

19-7809851-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809851
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809851
    reference: chr 19
allele count: 43
allele frequency: 3.542827011172264e-4
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.666C>T
  hgvsp: ENST00000593660.1:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.468C>T
  hgvsp: ENST00000301357.8:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.468C>T
  hgvsp: ENST00000593821.1:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.876C>T
  hgvsp: ENST00000354397.6:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.804C>T
  hgvsp: ENST00000601256.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.804C>T
  hgvsp: ENST00000601951.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.393C>T
  hgvsp: ENST00000394173.4:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.804C>T
  hgvsp: ENST00000315591.8:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.744C>T
  hgvsp: ENST00000204801.8:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.876C>T
  hgvsp: ENST00000315599.7:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-772C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.600C>T
  hgvsp: ENST00000602261.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val292Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

19-7809853-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809853
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809853
    reference: chr 19
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.742G>A
  hgvsp: ENSP00000204801.7:p.Val248Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.802G>A
  hgvsp: ENSP00000470658.1:p.Val268Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.874G>A
  hgvsp: ENSP00000315477.6:p.Val292Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.391G>A
  hgvsp: ENSP00000377728.4:p.Val131Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.874G>A
  hgvsp: ENSP00000346373.5:p.Val292Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.802G>A
  hgvsp: ENSP00000315407.7:p.Val268Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.466G>A
  hgvsp: ENSP00000471348.1:p.Val156Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-774G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.664G>A
  hgvsp: ENSP00000470530.1:p.Val222Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.598G>A
  hgvsp: ENSP00000471137.1:p.Val200Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.802G>A
  hgvsp: ENSP00000468827.1:p.Val268Ile
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.466G>A
  hgvsp: ENSP00000301357.8:p.Val156Ile
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val292Ile
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

19-7809854-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809854
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809854
    reference: chr 19
allele count: 10
allele frequency: 8.238318064983853e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.873C>T
  hgvsp: ENST00000354397.6:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.597C>T
  hgvsp: ENST00000602261.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.801C>T
  hgvsp: ENST00000601951.1:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.741C>T
  hgvsp: ENST00000204801.8:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.873C>T
  hgvsp: ENST00000315599.7:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.465C>T
  hgvsp: ENST00000301357.8:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.390C>T
  hgvsp: ENST00000394173.4:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.801C>T
  hgvsp: ENST00000601256.1:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.663C>T
  hgvsp: ENST00000593660.1:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-775C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.465C>T
  hgvsp: ENST00000593821.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.801C>T
  hgvsp: ENST00000315591.8:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu291Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-7809856-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809856
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809856
    reference: chr 19
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.871C>T
  hgvsp: ENSP00000346373.5:p.Leu291Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.388C>T
  hgvsp: ENSP00000377728.4:p.Leu130Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.799C>T
  hgvsp: ENSP00000470658.1:p.Leu267Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.661C>T
  hgvsp: ENSP00000470530.1:p.Leu221Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.463C>T
  hgvsp: ENSP00000471348.1:p.Leu155Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.871C>T
  hgvsp: ENSP00000315477.6:p.Leu291Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.739C>T
  hgvsp: ENSP00000204801.7:p.Leu247Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.799C>T
  hgvsp: ENSP00000468827.1:p.Leu267Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-777C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.799C>T
  hgvsp: ENSP00000315407.7:p.Leu267Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.595C>T
  hgvsp: ENSP00000471137.1:p.Leu199Phe
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.463C>T
  hgvsp: ENSP00000301357.8:p.Leu155Phe
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu291Phe
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

19-7809859-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809859
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809859
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.796C>T
  hgvsp: ENSP00000470658.1:p.Gln266Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.592C>T
  hgvsp: ENSP00000471137.1:p.Gln198Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.736C>T
  hgvsp: ENSP00000204801.7:p.Gln246Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.460C>T
  hgvsp: ENSP00000301357.8:p.Gln154Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.658C>T
  hgvsp: ENSP00000470530.1:p.Gln220Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.868C>T
  hgvsp: ENSP00000346373.5:p.Gln290Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.868C>T
  hgvsp: ENSP00000315477.6:p.Gln290Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.796C>T
  hgvsp: ENSP00000315407.7:p.Gln266Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-780C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.460C>T
  hgvsp: ENSP00000471348.1:p.Gln154Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.796C>T
  hgvsp: ENSP00000468827.1:p.Gln266Ter
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.385C>T
  hgvsp: ENSP00000377728.4:p.Gln129Ter
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8733
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln290Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

19-7809862-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809862
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809862
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.655G>A
  hgvsp: ENSP00000470530.1:p.Ala219Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.457G>A
  hgvsp: ENSP00000471348.1:p.Ala153Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.793G>A
  hgvsp: ENSP00000315407.7:p.Ala265Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.793G>A
  hgvsp: ENSP00000468827.1:p.Ala265Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.733G>A
  hgvsp: ENSP00000204801.7:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.865G>A
  hgvsp: ENSP00000315477.6:p.Ala289Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.865G>A
  hgvsp: ENSP00000346373.5:p.Ala289Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.457G>A
  hgvsp: ENSP00000301357.8:p.Ala153Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-783G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.793G>A
  hgvsp: ENSP00000470658.1:p.Ala265Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.382G>A
  hgvsp: ENSP00000377728.4:p.Ala128Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.589G>A
  hgvsp: ENSP00000471137.1:p.Ala197Thr
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala289Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

19-7809865-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809865
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809865
    reference: chr 19
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.730G>A
  hgvsp: ENSP00000204801.7:p.Gly244Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.790G>A
  hgvsp: ENSP00000468827.1:p.Gly264Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-786G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.790G>A
  hgvsp: ENSP00000315407.7:p.Gly264Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.454G>A
  hgvsp: ENSP00000471348.1:p.Gly152Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.379G>A
  hgvsp: ENSP00000377728.4:p.Gly127Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.586G>A
  hgvsp: ENSP00000471137.1:p.Gly196Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.652G>A
  hgvsp: ENSP00000470530.1:p.Gly218Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.862G>A
  hgvsp: ENSP00000315477.6:p.Gly288Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.790G>A
  hgvsp: ENSP00000470658.1:p.Gly264Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.454G>A
  hgvsp: ENSP00000301357.8:p.Gly152Arg
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.862G>A
  hgvsp: ENSP00000346373.5:p.Gly288Arg
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly288Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-7809872-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809872
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809872
    reference: chr 19
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.723A>G
  hgvsp: ENST00000204801.8:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.783A>G
  hgvsp: ENST00000315591.8:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.579A>G
  hgvsp: ENST00000602261.1:c.579A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.447A>G
  hgvsp: ENST00000593821.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-793A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.783A>G
  hgvsp: ENST00000601256.1:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.855A>G
  hgvsp: ENST00000315599.7:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.855A>G
  hgvsp: ENST00000354397.6:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.447A>G
  hgvsp: ENST00000301357.8:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.645A>G
  hgvsp: ENST00000593660.1:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.783A>G
  hgvsp: ENST00000601951.1:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.372A>G
  hgvsp: ENST00000394173.4:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys285Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-7809874-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809874
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809874
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.445A>C
  hgvsp: ENSP00000471348.1:p.Lys149Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.445A>C
  hgvsp: ENSP00000301357.8:p.Lys149Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.781A>C
  hgvsp: ENSP00000470658.1:p.Lys261Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.781A>C
  hgvsp: ENSP00000468827.1:p.Lys261Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.853A>C
  hgvsp: ENSP00000315477.6:p.Lys285Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.577A>C
  hgvsp: ENSP00000471137.1:p.Lys193Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.853A>C
  hgvsp: ENSP00000346373.5:p.Lys285Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.370A>C
  hgvsp: ENSP00000377728.4:p.Lys124Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.721A>C
  hgvsp: ENSP00000204801.7:p.Lys241Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.781A>C
  hgvsp: ENSP00000315407.7:p.Lys261Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.643A>C
  hgvsp: ENSP00000470530.1:p.Lys215Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-795A>C
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys285Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

19-7809880-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809880
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809880
    reference: chr 19
allele count: 17
allele frequency: 1.400329489291598e-4
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.847G>A
  hgvsp: ENSP00000346373.5:p.Ala283Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.775G>A
  hgvsp: ENSP00000468827.1:p.Ala259Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.715G>A
  hgvsp: ENSP00000204801.7:p.Ala239Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.637G>A
  hgvsp: ENSP00000470530.1:p.Ala213Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.439G>A
  hgvsp: ENSP00000471348.1:p.Ala147Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-801G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.847G>A
  hgvsp: ENSP00000315477.6:p.Ala283Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.439G>A
  hgvsp: ENSP00000301357.8:p.Ala147Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.571G>A
  hgvsp: ENSP00000471137.1:p.Ala191Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.775G>A
  hgvsp: ENSP00000470658.1:p.Ala259Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.364G>A
  hgvsp: ENSP00000377728.4:p.Ala122Thr
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.775G>A
  hgvsp: ENSP00000315407.7:p.Ala259Thr
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ala283Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

19-7809881-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809881
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809881
    reference: chr 19
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.438C>T
  hgvsp: ENST00000301357.8:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.846C>T
  hgvsp: ENST00000315599.7:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-802C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.774C>T
  hgvsp: ENST00000601256.1:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.438C>T
  hgvsp: ENST00000593821.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.363C>T
  hgvsp: ENST00000394173.4:c.363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.714C>T
  hgvsp: ENST00000204801.8:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.774C>T
  hgvsp: ENST00000601951.1:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.774C>T
  hgvsp: ENST00000315591.8:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.570C>T
  hgvsp: ENST00000602261.1:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.636C>T
  hgvsp: ENST00000593660.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.846C>T
  hgvsp: ENST00000354397.6:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr282Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

19-7809886-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809886
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809886
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.841A>G
  hgvsp: ENSP00000346373.5:p.Ile281Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.631A>G
  hgvsp: ENSP00000470530.1:p.Ile211Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.433A>G
  hgvsp: ENSP00000471348.1:p.Ile145Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.433A>G
  hgvsp: ENSP00000301357.8:p.Ile145Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-807A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.769A>G
  hgvsp: ENSP00000468827.1:p.Ile257Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.358A>G
  hgvsp: ENSP00000377728.4:p.Ile120Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.769A>G
  hgvsp: ENSP00000470658.1:p.Ile257Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.769A>G
  hgvsp: ENSP00000315407.7:p.Ile257Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.841A>G
  hgvsp: ENSP00000315477.6:p.Ile281Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.709A>G
  hgvsp: ENSP00000204801.7:p.Ile237Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.565A>G
  hgvsp: ENSP00000471137.1:p.Ile189Val
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile281Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-7809891-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809891
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809891
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.764A>T
  hgvsp: ENSP00000470658.1:p.Asp255Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.626A>T
  hgvsp: ENSP00000470530.1:p.Asp209Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.836A>T
  hgvsp: ENSP00000346373.5:p.Asp279Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.353A>T
  hgvsp: ENSP00000377728.4:p.Asp118Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.560A>T
  hgvsp: ENSP00000471137.1:p.Asp187Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.764A>T
  hgvsp: ENSP00000468827.1:p.Asp255Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.428A>T
  hgvsp: ENSP00000471348.1:p.Asp143Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.704A>T
  hgvsp: ENSP00000204801.7:p.Asp235Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.428A>T
  hgvsp: ENSP00000301357.8:p.Asp143Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.764A>T
  hgvsp: ENSP00000315407.7:p.Asp255Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.836A>T
  hgvsp: ENSP00000315477.6:p.Asp279Val
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-812A>T
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp279Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

19-7809892-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809892
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809892
    reference: chr 19
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.352G>A
  hgvsp: ENSP00000377728.4:p.Asp118Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.835G>A
  hgvsp: ENSP00000346373.5:p.Asp279Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-813G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.763G>A
  hgvsp: ENSP00000315407.7:p.Asp255Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.427G>A
  hgvsp: ENSP00000301357.8:p.Asp143Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.763G>A
  hgvsp: ENSP00000470658.1:p.Asp255Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.703G>A
  hgvsp: ENSP00000204801.7:p.Asp235Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.559G>A
  hgvsp: ENSP00000471137.1:p.Asp187Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.427G>A
  hgvsp: ENSP00000471348.1:p.Asp143Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.625G>A
  hgvsp: ENSP00000470530.1:p.Asp209Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.835G>A
  hgvsp: ENSP00000315477.6:p.Asp279Asn
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.763G>A
  hgvsp: ENSP00000468827.1:p.Asp255Asn
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5135
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp279Asn
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

19-7809893-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809893
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809893
    reference: chr 19
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.558C>T
  hgvsp: ENST00000602261.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.834C>T
  hgvsp: ENST00000315599.7:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.426C>T
  hgvsp: ENST00000301357.8:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.762C>T
  hgvsp: ENST00000601951.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-814C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.762C>T
  hgvsp: ENST00000315591.8:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.624C>T
  hgvsp: ENST00000593660.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.351C>T
  hgvsp: ENST00000394173.4:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.762C>T
  hgvsp: ENST00000601256.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.702C>T
  hgvsp: ENST00000204801.8:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.834C>T
  hgvsp: ENST00000354397.6:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.426C>T
  hgvsp: ENST00000593821.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His278His
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

19-7809901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809901
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809901
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.343A>G
  hgvsp: ENSP00000377728.4:p.Asn115Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.754A>G
  hgvsp: ENSP00000315407.7:p.Asn252Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.754A>G
  hgvsp: ENSP00000470658.1:p.Asn252Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.616A>G
  hgvsp: ENSP00000470530.1:p.Asn206Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-822A>G
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.418A>G
  hgvsp: ENSP00000301357.8:p.Asn140Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.694A>G
  hgvsp: ENSP00000204801.7:p.Asn232Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.754A>G
  hgvsp: ENSP00000468827.1:p.Asn252Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.826A>G
  hgvsp: ENSP00000315477.6:p.Asn276Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.418A>G
  hgvsp: ENSP00000471348.1:p.Asn140Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.826A>G
  hgvsp: ENSP00000346373.5:p.Asn276Asp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.550A>G
  hgvsp: ENSP00000471137.1:p.Asn184Asp
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn276Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

19-7809903-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809903
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809903
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.752G>A
  hgvsp: ENSP00000315407.7:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.824G>A
  hgvsp: ENSP00000346373.5:p.Arg275Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.614G>A
  hgvsp: ENSP00000470530.1:p.Arg205Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.824G>A
  hgvsp: ENSP00000315477.6:p.Arg275Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.692G>A
  hgvsp: ENSP00000204801.7:p.Arg231Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.416G>A
  hgvsp: ENSP00000301357.8:p.Arg139Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.548G>A
  hgvsp: ENSP00000471137.1:p.Arg183Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.416G>A
  hgvsp: ENSP00000471348.1:p.Arg139Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.752G>A
  hgvsp: ENSP00000470658.1:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.341G>A
  hgvsp: ENSP00000377728.4:p.Arg114Gln
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-824G>A
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.752G>A
  hgvsp: ENSP00000468827.1:p.Arg251Gln
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg275Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

19-7809904-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7809904
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 7809904
    reference: chr 19
allele count: 11
allele frequency: 9.060209208467177e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470658
  ensembl transcript: ENST00000601256
  gene symbol: CD209
  hgvsc: ENST00000601256.1:c.751C>T
  hgvsp: ENSP00000470658.1:p.Arg251Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315407
  ensembl transcript: ENST00000315591
  gene symbol: CD209
  hgvsc: ENST00000315591.8:c.751C>T
  hgvsp: ENSP00000315407.7:p.Arg251Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000204801
  ensembl transcript: ENST00000204801
  gene symbol: CD209
  hgvsc: ENST00000204801.8:c.691C>T
  hgvsp: ENSP00000204801.7:p.Arg231Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000301357
  ensembl transcript: ENST00000301357
  gene symbol: CD209
  hgvsc: ENST00000301357.8:c.415C>T
  hgvsp: ENSP00000301357.8:p.Arg139Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000315477
  ensembl transcript: ENST00000315599
  gene symbol: CD209
  hgvsc: ENST00000315599.7:c.823C>T
  hgvsp: ENSP00000315477.6:p.Arg275Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377728
  ensembl transcript: ENST00000394173
  gene symbol: CD209
  hgvsc: ENST00000394173.4:c.340C>T
  hgvsp: ENSP00000377728.4:p.Arg114Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471137
  ensembl transcript: ENST00000602261
  gene symbol: CD209
  hgvsc: ENST00000602261.1:c.547C>T
  hgvsp: ENSP00000471137.1:p.Arg183Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000471348
  ensembl transcript: ENST00000593821
  gene symbol: CD209
  hgvsc: ENST00000593821.1:c.415C>T
  hgvsp: ENSP00000471348.1:p.Arg139Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000470530
  ensembl transcript: ENST00000593660
  gene symbol: CD209
  hgvsc: ENST00000593660.1:c.613C>T
  hgvsp: ENSP00000470530.1:p.Arg205Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000346373
  ensembl transcript: ENST00000354397
  gene symbol: CD209
  hgvsc: ENST00000354397.6:c.823C>T
  hgvsp: ENSP00000346373.5:p.Arg275Trp
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000377716
  ensembl transcript: ENST00000394161
  gene symbol: CD209
  hgvsc: ENST00000394161.5:c.219-825C>T
  variant of: http://identifiers.org/hgnc/1641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090659
  ensembl protein: ENSP00000468827
  ensembl transcript: ENST00000601951
  gene symbol: CD209
  hgvsc: ENST00000601951.1:c.751C>T
  hgvsp: ENSP00000468827.1:p.Arg251Trp
  variant of: http://identifiers.org/hgnc/1641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg275Trp
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 6113
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1794
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3856
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1831
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4796
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9760
bin: 9.75e1
variant carriers: 1

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

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

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

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

GenotypeQuality
all individuals: 2463
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25852
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.629999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.477e0

MQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-1

DP
type: SiteQuality
SIO_000300: 1.980038e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

GenotypeDepth
all individuals: 11676
bin: 3.25e1
variant carriers: 5

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

GenotypeDepth
all individuals: 148
bin: 9.25e1
variant carriers: 68

GenotypeDepth
all individuals: 750
bin: 5.75e1
variant carriers: 53

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

GenotypeQuality
all individuals: 25580
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3548
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1786
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8388
bin: 6.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10532
bin: 9.75e1
variant carriers: 1027

GenotypeQuality
all individuals: 4693
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 11
allele frequency: 1.057488944433763e-3
allele num: 10402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 71
allele frequency: 1.07348049591775e-2
allele num: 6614
num of homozygotes: 1

Other
type: Population
allele count: 10
allele frequency: 1.101321585903084e-2
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 103
allele frequency: 6.237887596899225e-3
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 45
allele frequency: 3.88668163758853e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 792
allele frequency: 1.186801330656037e-2
allele num: 66734
num of homozygotes: 5

DP
type: SiteQuality
SIO_000300: 2.04091e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

FS
type: SiteQuality
SIO_000300: 1.253e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 1.265e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

GenotypeDepth
all individuals: 11934
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1056
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4779
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3808
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8545
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25970
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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MQRankSum
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MQ
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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European (Finnish)
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Other
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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African
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FS
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QD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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Latino
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East Asian
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African
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European (Non-Finnish)
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FS
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DP
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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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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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African
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Latino
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East Asian
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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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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Latino
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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East Asian
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South Asian
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Other
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FS
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VQSLOD
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QD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
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East Asian
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allele frequency: 0.0e0
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Latino
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South Asian
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African
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allele num: 10406
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Other
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQ
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MQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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num of homozygotes: 0

East Asian
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allele num: 8654
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Other
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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QD
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VQSLOD
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FS
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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East Asian
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allele num: 8654
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 908
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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num of homozygotes: 0

African
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South Asian
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East Asian
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European (Non-Finnish)
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allele num: 66740
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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QD
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MQ
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VQSLOD
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FS
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MQRankSum
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 31

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

East Asian
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allele frequency: 4.968800554656806e-3
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African
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Other
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European (Non-Finnish)
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allele frequency: 8.990110878034162e-5
allele num: 66740
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 66738
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South Asian
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DP
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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QD
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MQ
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SIO_000300: 5.893e1

ReadPosRankSum
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SIO_000300: 1.88e0

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

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

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

European (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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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 (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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FS
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BaseQRankSum
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SIO_000300: 1.78e-1

DP
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SIO_000300: 1.98632e6

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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East 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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

MQRankSum
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VQSLOD
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QD
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SIO_000300: 1.068e1

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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DP
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SIO_000300: 1.98632e6

BaseQRankSum
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SIO_000300: 1.78e-1

FS
type: SiteQuality
SIO_000300: 1.3151e1

GenotypeDepth
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variant carriers: 96

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 84

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

South Asian
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allele count: 26
allele frequency: 1.574993942330991e-3
allele num: 16508
num of homozygotes: 0

Latino
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allele count: 125
allele frequency: 1.079820317899102e-2
allele num: 11576
num of homozygotes: 2

European (Finnish)
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allele frequency: 1.209555488358028e-3
allele num: 6614
num of homozygotes: 0

East Asian
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Other
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allele frequency: 5.506607929515419e-3
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num of homozygotes: 0

African
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allele count: 1198
allele frequency: 1.151258889102441e-1
allele num: 10406
num of homozygotes: 71

European (Non-Finnish)
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allele count: 307
allele frequency: 4.600077916629207e-3
allele num: 66738
num of homozygotes: 2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

FS
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DP
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MQRankSum
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MQ
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SIO_000300: 5.527e1

VQSLOD
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ClippingRankSum
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SIO_000300: 2.51e-1

QD
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BaseQRankSum
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SIO_000300: 3.03e0

InbreedingCoeff
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SIO_000300: 7.51e-2

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

African
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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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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East Asian
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European (Non-Finnish)
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allele num: 66732
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BaseQRankSum
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VQSLOD
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DP
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FS
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ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

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

Other
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Latino
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European (Finnish)
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South Asian
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African
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East Asian
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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DP
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

European (Non-Finnish)
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Other
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South Asian
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East Asian
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Latino
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.116e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.272e0

DP
type: SiteQuality
SIO_000300: 2.048451e6

VQSLOD
type: SiteQuality
SIO_000300: -1.978e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.06e-1

FS
type: SiteQuality
SIO_000300: 3.883e0

QD
type: SiteQuality
SIO_000300: 1.453e1

GenotypeDepth
all individuals: 118
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variant carriers: 0

GenotypeDepth
all individuals: 346
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2445
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3728
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.44e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.92e-1

DP
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SIO_000300: 2.044658e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

QD
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SIO_000300: 1.173e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

GenotypeDepth
all individuals: 1303
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4673
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.50030001200048e-5
allele num: 66664
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.454e1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

FS
type: SiteQuality
SIO_000300: 6.47e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 2.044854e6

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.75e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 4679
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3487
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000750187546887e-5
allele num: 66650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 2.65e1

DP
type: SiteQuality
SIO_000300: 2.042968e6

VQSLOD
type: SiteQuality
SIO_000300: -2.881e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

FS
type: SiteQuality
SIO_000300: 3.293e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e0

GenotypeDepth
all individuals: 1300
bin: 9.75e1
variant carriers: 283

GenotypeQuality
all individuals: 10731
bin: 9.75e1
variant carriers: 1590

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 8010
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2371
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GenotypeQuality
all individuals: 3393
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.584013646886804e-3
allele num: 16414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 308
allele frequency: 4.625319116984532e-3
allele num: 66590
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.211020284589767e-3
allele num: 6606
num of homozygotes: 0

Latino
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allele count: 125
allele frequency: 1.081501989963662e-2
allele num: 11558
num of homozygotes: 2

African
type: Population
allele count: 1198
allele frequency: 1.152144643200615e-1
allele num: 10398
num of homozygotes: 71

Other
type: Population
allele count: 5
allele frequency: 5.543237250554324e-3
allele num: 902
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.295e1

FS
type: SiteQuality
SIO_000300: 7.46e-1

MQRankSum
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SIO_000300: -3.473e0

InbreedingCoeff
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SIO_000300: 7.190000000000001e-2

QD
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SIO_000300: 1.455e1

BaseQRankSum
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SIO_000300: -7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 2.036845e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9596
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.233e0

ClippingRankSum
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SIO_000300: 1.96e0

MQRankSum
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MQ
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DP
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ReadPosRankSum
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SIO_000300: 1.17e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.701e0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.63e-1

VQSLOD
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SIO_000300: 6.81e-1

InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.232e0

DP
type: SiteQuality
SIO_000300: 1.964695e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 863
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GenotypeQuality
all individuals: 1752
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506205566935775e-5
allele num: 66392
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.064e0

InbreedingCoeff
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SIO_000300: 3.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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QD
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VQSLOD
type: SiteQuality
SIO_000300: -5.442e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.934662e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

MQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.028636021100226e-5
allele num: 66350
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 9.320000000000001e-1

InbreedingCoeff
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SIO_000300: 3.9e-3

ClippingRankSum
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DP
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FS
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.273e0

ReadPosRankSum
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SIO_000300: 3.9e-2

QD
type: SiteQuality
SIO_000300: 1.225e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 4.816955684007707e-4
allele num: 10380
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

DP
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ClippingRankSum
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MQ
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FS
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MQRankSum
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VQSLOD
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SIO_000300: 9.72e-1

QD
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SIO_000300: 1.391e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

BaseQRankSum
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SIO_000300: -2.03e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.152331733727083e-5
allele num: 16254
num of homozygotes: 0

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

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
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 1.45e0

DP
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SIO_000300: 1.912523e6

MQRankSum
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SIO_000300: 5.659999999999999e-1

InbreedingCoeff
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SIO_000300: 3.5e-3

FS
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VQSLOD
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BaseQRankSum
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SIO_000300: -2.262e0

QD
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SIO_000300: 9.73e0

ReadPosRankSum
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66204
num of homozygotes: 0

Other
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South Asian
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allele num: 16228
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Latino
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African
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allele frequency: 0.0e0
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European (Finnish)
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MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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East Asian
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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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European (Non-Finnish)
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MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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Latino
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African
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Other
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MQ
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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VQSLOD
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele num: 66274
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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African
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East Asian
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European (Finnish)
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South Asian
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BaseQRankSum
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FS
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

East Asian
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allele count: 4
allele frequency: 4.624277456647399e-4
allele num: 8650
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66304
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

DP
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SIO_000300: 2.541997e6

ClippingRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.575e0

FS
type: SiteQuality
SIO_000300: 1.517e0

QD
type: SiteQuality
SIO_000300: 1.345e1

GenotypeDepth
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variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507840772014475e-5
allele num: 66320
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15792
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: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 2.26e-2

ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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SIO_000300: -1.256e0

MQ
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SIO_000300: 5.962e1

QD
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SIO_000300: 1.54e1

MQRankSum
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SIO_000300: 2.3e0

ReadPosRankSum
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SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 2.544412e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2334
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.333924499619965e-5
allele num: 15788
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -6.830000000000001e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -3.266e0

MQRankSum
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SIO_000300: -7.58e-1

VQSLOD
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SIO_000300: 3.19e-1

DP
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SIO_000300: 2.546549e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 1.624e1

GenotypeDepth
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variant carriers: 18

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 159

GenotypeQuality
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GenotypeQuality
all individuals: 146
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variant carriers: 0

GenotypeQuality
all individuals: 2367
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 97
allele frequency: 1.460931381408519e-3
allele num: 66396
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.925669170036588e-4
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.123789764868603e-3
allele num: 11568
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.348214285714286e-3
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 43
allele frequency: 2.694573254793834e-3
allele num: 15958
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
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SIO_000300: 2.18e-2

VQSLOD
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SIO_000300: 1.66e0

MQRankSum
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SIO_000300: 2.76e-1

DP
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SIO_000300: 2.560458e6

BaseQRankSum
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SIO_000300: -1.647e0

FS
type: SiteQuality
SIO_000300: 4.108e0

QD
type: SiteQuality
SIO_000300: 1.154e1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 13

GenotypeDepth
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variant carriers: 11

GenotypeQuality
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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: 28700
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variant carriers: 128

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 50
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GenotypeQuality
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GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 2302
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003634397621121e-5
allele num: 66586
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.119202056051891e-5
allele num: 16342
num of homozygotes: 0

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

African
type: Population
allele count: 124
allele frequency: 1.192307692307692e-2
allele num: 10400
num of homozygotes: 2

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

DP
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SIO_000300: 2.57807e6

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
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SIO_000300: 2.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.55e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

QD
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SIO_000300: 1.282e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2304
bin: 8.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Latino
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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: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

South Asian
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allele count: 0
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allele num: 16468
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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BaseQRankSum
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MQ
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SIO_000300: 5.93e1

InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.877e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 5.084e0

ReadPosRankSum
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BaseQRankSum
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SIO_000300: 2.69e0

MQ
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SIO_000300: 5.946e1

QD
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GenotypeDepth
all individuals: 967
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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ClippingRankSum
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Other
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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ReadPosRankSum
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QD
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BaseQRankSum
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VQSLOD
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DP
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 66690
num of homozygotes: 0

European (Finnish)
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Other
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African
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Latino
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East Asian
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South Asian
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

South Asian
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Latino
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European (Non-Finnish)
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Other
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African
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allele frequency: 2.114164904862579e-3
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European (Finnish)
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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QD
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VQSLOD
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BaseQRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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Latino
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African
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South Asian
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East Asian
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European (Non-Finnish)
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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DP
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MQRankSum
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MQ
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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Other
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European (Finnish)
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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SIO_000300: -1.363e0

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.927e1

FS
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SIO_000300: 1.134e0

ReadPosRankSum
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SIO_000300: 5.44e-1

QD
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VQSLOD
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DP
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SIO_000300: 2.582379e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.04e-1

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
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allele num: 8654
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.049223574554829e-4
allele num: 66716
num of homozygotes: 0

South Asian
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ClippingRankSum
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SIO_000300: -1.05e-1

FS
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: 1.01e-1

DP
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SIO_000300: 2.582763e6

BaseQRankSum
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SIO_000300: 1.47e0

ReadPosRankSum
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SIO_000300: 3.02e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66716
num of homozygotes: 0

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

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

Latino
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 2.582642e6

MQRankSum
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SIO_000300: 7.31e-1

BaseQRankSum
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SIO_000300: -2.983e0

VQSLOD
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SIO_000300: 2.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.58e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66724
num of homozygotes: 0

Latino
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num of homozygotes: 0

MQRankSum
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SIO_000300: 1.78e0

QD
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ReadPosRankSum
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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DP
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ClippingRankSum
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SIO_000300: -2.0e-2

BaseQRankSum
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SIO_000300: -2.256e0

GenotypeDepth
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variant carriers: 0

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

Other
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num of homozygotes: 0

South Asian
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Latino
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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MQRankSum
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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ReadPosRankSum
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QD
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BaseQRankSum
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MQ
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VQSLOD
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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num of homozygotes: 0

African
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Latino
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Other
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East Asian
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South Asian
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 8654
num of homozygotes: 0

European (Finnish)
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Other
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Latino
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African
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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QD
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ReadPosRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.582795e6

FS
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SIO_000300: 5.459e0

ClippingRankSum
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SIO_000300: 1.54e0

ReadPosRankSum
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MQRankSum
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SIO_000300: -3.319e0

MQ
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SIO_000300: 5.827e1

BaseQRankSum
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VQSLOD
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QD
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SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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: 8
allele frequency: 7.68787238131847e-4
allele num: 10406
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

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 (Non-Finnish)
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allele frequency: 1.348637875745497e-4
allele num: 66734
num of homozygotes: 0

East Asian
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num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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QD
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VQSLOD
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FS
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SIO_000300: 1.104e0

ReadPosRankSum
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MQ
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SIO_000300: 5.952e1

ClippingRankSum
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SIO_000300: -6.98e-1

GenotypeDepth
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variant carriers: 0

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

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

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 num: 11576
num of homozygotes: 0

East Asian
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Other
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num of homozygotes: 0

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

South Asian
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BaseQRankSum
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SIO_000300: 1.79e0

VQSLOD
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InbreedingCoeff
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FS
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SIO_000300: 1.032e0

QD
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ClippingRankSum
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ReadPosRankSum
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DP
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SIO_000300: 2.583006e6

MQRankSum
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SIO_000300: 5.94e-1

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

East Asian
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allele num: 8654
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

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

VQSLOD
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SIO_000300: -4.9e0

BaseQRankSum
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MQRankSum
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FS
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DP
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

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

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

European (Finnish)
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South Asian
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Other
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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FS
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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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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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
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ClippingRankSum
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QD
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FS
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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Other
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South Asian
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African
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European (Finnish)
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VQSLOD
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ClippingRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 2306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28610
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10561
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4006
bin: 9.25e1
variant carriers: 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: 908
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
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: 10406
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

MQ
type: SiteQuality
SIO_000300: 5.889e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

QD
type: SiteQuality
SIO_000300: 1.275e1

DP
type: SiteQuality
SIO_000300: 2.582956e6

FS
type: SiteQuality
SIO_000300: 3.035e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.92e-1

GenotypeDepth
all individuals: 286
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4630
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10558
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4005
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4006
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28609
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 10406
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

DP
type: SiteQuality
SIO_000300: 2.582993e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e-1

FS
type: SiteQuality
SIO_000300: 1.503e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeDepth
all individuals: 8736
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 287
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 967
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1438
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4628
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4006
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2306
bin: 8.75e1
variant carriers: 0

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