11-44621774-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44621774
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44621774
    reference: chr 11
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.322G>A
  hgvsp: ENSP00000433151.1:p.Val108Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.130G>A
  hgvsp: ENSP00000431767.1:p.Val44Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.130G>A
  hgvsp: ENSP00000433804.1:p.Val44Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.130G>A
  hgvsp: ENSP00000339686.3:p.Val44Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.130G>A
  hgvsp: ENSP00000436403.1:p.Val44Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.130G>A
  hgvsp: ENSP00000227155.4:p.Val44Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.302G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.253G>A
  hgvsp: ENSP00000435682.1:p.Val85Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.73G>A
  hgvsp: ENSP00000433788.1:p.Val25Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.124+12721G>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val44Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

11-44621780-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44621780
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44621780
    reference: chr 11
allele count: 9
allele frequency: 7.418642223614363e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.79C>T
  hgvsp: ENSP00000433788.1:p.Gln27Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.136C>T
  hgvsp: ENSP00000227155.4:p.Gln46Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.136C>T
  hgvsp: ENSP00000339686.3:p.Gln46Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.136C>T
  hgvsp: ENSP00000431767.1:p.Gln46Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.328C>T
  hgvsp: ENSP00000433151.1:p.Gln110Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.136C>T
  hgvsp: ENSP00000436403.1:p.Gln46Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.124+12727C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.308C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.136C>T
  hgvsp: ENSP00000433804.1:p.Gln46Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.259C>T
  hgvsp: ENSP00000435682.1:p.Gln87Ter
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln46Ter
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

11-44621792-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44621792
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44621792
    reference: chr 11
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.136+12T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.136+12T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.124+12739T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.136+12T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.328+12T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.136+12T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.259+12T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.136+12T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.79+12T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.308+12T>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5567
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

11-44621794-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44621794
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44621794
    reference: chr 11
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.124+12741A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.136+14A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.79+14A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.136+14A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.136+14A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.308+14A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.328+14A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.136+14A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.259+14A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.136+14A>G
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13686
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

11-44621804-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44621804
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44621804
    reference: chr 11
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.328+24G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.79+24G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.136+24G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.308+24G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.136+24G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.136+24G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.136+24G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.124+12751G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.259+24G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.136+24G>C
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

11-44621806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44621806
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44621806
    reference: chr 11
allele count: 6
allele frequency: 4.952701698776683e-5
allele num: 121146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.328+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.259+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.136+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.124+12753C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.136+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.136+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.308+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.136+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.136+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.79+26C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2371
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5487
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-44621807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44621807
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44621807
    reference: chr 11
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.79+27C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.124+12754C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.328+27C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.308+27C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.136+27C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.136+27C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.136+27C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.136+27C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.259+27C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.136+27C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13395
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5477
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4692
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-44626567-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626567
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626567
    reference: chr 11
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.320+1G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13261C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-41C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-41C>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14144
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.320+1G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

11-44626567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626567
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626567
    reference: chr 11
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.320+1G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13261C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-41C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-41C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: n.320+1G>A
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

11-44626576-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626576
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626576
    reference: chr 11
allele count: 3
allele frequency: 2.47222863170386e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13252C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.312G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-32C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-32C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15011
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-44626582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626582
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626582
    reference: chr 11
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13246G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.306C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-26G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-26G>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

11-44626584-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626584
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626584
    reference: chr 11
allele count: 3
allele frequency: 2.472147142197904e-5
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.304A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13244T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-24T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-24T>G
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-44626587-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626587
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626587
    reference: chr 11
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.301A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13241T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-21T>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-21T>G
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

11-44626590-ACTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626590
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626587
    reference: chr 11
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-10_329-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.295_297delAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-10_75-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-10_80-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-10_137-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-10_137-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-10_137-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-10_137-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-10_137-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-10_260-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-10_309-8delTTC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13230_125-13228delTTC
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: ACTT
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

11-44626593-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626593
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626593
    reference: chr 11
allele count: 1676
allele frequency: 1.380969645034771e-2
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.295A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-15T>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13235T>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14146
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 9.75e1
  variant carriers: 1385
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 15060
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9106
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 45
genotype quality: GenotypeQuality
num of homozygotes: 21
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/11-44626603-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626603
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626603
    reference: chr 11
allele count: 9
allele frequency: 7.41485277397881e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.285G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.137-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.80-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.137-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.329-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.137-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.309-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.75-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13225C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.137-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.260-5C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.137-5C>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.137-5C>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-44626614-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626614
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626614
    reference: chr 11
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.86C>T
  hgvsp: ENSP00000433788.1:p.Ser29Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.143C>T
  hgvsp: ENSP00000339686.3:p.Ser48Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.143C>T
  hgvsp: ENSP00000433804.1:p.Ser48Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.266C>T
  hgvsp: ENSP00000435682.1:p.Ser89Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13214C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.143C>T
  hgvsp: ENSP00000227155.4:p.Ser48Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.335C>T
  hgvsp: ENSP00000433151.1:p.Ser112Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.81C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.143C>T
  hgvsp: ENSP00000431767.1:p.Ser48Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.143C>T
  hgvsp: ENSP00000436403.1:p.Ser48Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.315C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.274G>A
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser48Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/11-44626623-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626623
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626623
    reference: chr 11
allele count: 2
allele frequency: 1.647799363949445e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.152C>A
  hgvsp: ENSP00000433804.1:p.Ser51Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.344C>A
  hgvsp: ENSP00000433151.1:p.Ser115Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.152C>A
  hgvsp: ENSP00000339686.3:p.Ser51Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.95C>A
  hgvsp: ENSP00000433788.1:p.Ser32Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.152C>A
  hgvsp: ENSP00000227155.4:p.Ser51Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.265G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.90C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.275C>A
  hgvsp: ENSP00000435682.1:p.Ser92Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13205C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.152C>A
  hgvsp: ENSP00000431767.1:p.Ser51Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.152C>A
  hgvsp: ENSP00000436403.1:p.Ser51Ter
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.324C>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser51Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

11-44626624-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626624
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626624
    reference: chr 11
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.91G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.153G>A
  hgvsp: ENST00000342935.3:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.96G>A
  hgvsp: ENST00000530601.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.153G>A
  hgvsp: ENST00000227155.4:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.276G>A
  hgvsp: ENST00000526958.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.264C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.153G>A
  hgvsp: ENST00000525813.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.345G>A
  hgvsp: ENST00000527737.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.153G>A
  hgvsp: ENST00000532544.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.325G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13204G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.153G>A
  hgvsp: ENST00000524704.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser51Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-44626630-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626630
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626630
    reference: chr 11
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.159G>T
  hgvsp: ENSP00000339686.3:p.Arg53Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.102G>T
  hgvsp: ENSP00000433788.1:p.Arg34Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.159G>T
  hgvsp: ENSP00000433804.1:p.Arg53Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13198G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.282G>T
  hgvsp: ENSP00000435682.1:p.Arg94Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.97G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.159G>T
  hgvsp: ENSP00000431767.1:p.Arg53Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.258C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.351G>T
  hgvsp: ENSP00000433151.1:p.Arg117Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.159G>T
  hgvsp: ENSP00000227155.4:p.Arg53Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.331G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.159G>T
  hgvsp: ENSP00000436403.1:p.Arg53Ser
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg53Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

11-44626640-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626640
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626640
    reference: chr 11
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.292T>C
  hgvsp: ENSP00000435682.1:p.Tyr98His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.361T>C
  hgvsp: ENSP00000433151.1:p.Tyr121His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.341T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13188T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.169T>C
  hgvsp: ENSP00000227155.4:p.Tyr57His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.169T>C
  hgvsp: ENSP00000436403.1:p.Tyr57His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.169T>C
  hgvsp: ENSP00000339686.3:p.Tyr57His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.169T>C
  hgvsp: ENSP00000431767.1:p.Tyr57His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.169T>C
  hgvsp: ENSP00000433804.1:p.Tyr57His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.112T>C
  hgvsp: ENSP00000433788.1:p.Tyr38His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.107T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.248A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr57His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

11-44626642-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626642
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626642
    reference: chr 11
allele count: 17
allele frequency: 1.400444847186754e-4
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.171T>C
  hgvsp: ENST00000342935.3:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.171T>C
  hgvsp: ENST00000532544.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.294T>C
  hgvsp: ENST00000526958.1:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.171T>C
  hgvsp: ENST00000227155.4:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.171T>C
  hgvsp: ENST00000524704.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.171T>C
  hgvsp: ENST00000525813.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.343T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.363T>C
  hgvsp: ENST00000527737.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13186T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.114T>C
  hgvsp: ENST00000530601.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.109T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.246A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr57Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-44626643-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626643
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626643
    reference: chr 11
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.110G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.172G>A
  hgvsp: ENSP00000339686.3:p.Val58Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.295G>A
  hgvsp: ENSP00000435682.1:p.Val99Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.364G>A
  hgvsp: ENSP00000433151.1:p.Val122Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.115G>A
  hgvsp: ENSP00000433788.1:p.Val39Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.172G>A
  hgvsp: ENSP00000436403.1:p.Val58Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.172G>A
  hgvsp: ENSP00000227155.4:p.Val58Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.245C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.172G>A
  hgvsp: ENSP00000431767.1:p.Val58Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.344G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.172G>A
  hgvsp: ENSP00000433804.1:p.Val58Ile
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13185G>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val58Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

11-44626651-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626651
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626651
    reference: chr 11
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.118C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.180C>G
  hgvsp: ENSP00000436403.1:p.Ile60Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.180C>G
  hgvsp: ENSP00000339686.3:p.Ile60Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.180C>G
  hgvsp: ENSP00000227155.4:p.Ile60Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.372C>G
  hgvsp: ENSP00000433151.1:p.Ile124Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.180C>G
  hgvsp: ENSP00000431767.1:p.Ile60Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.303C>G
  hgvsp: ENSP00000435682.1:p.Ile101Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.237G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.352C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13177C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.123C>G
  hgvsp: ENSP00000433788.1:p.Ile41Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.180C>G
  hgvsp: ENSP00000433804.1:p.Ile60Met
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile60Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

11-44626651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626651
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626651
    reference: chr 11
allele count: 8
allele frequency: 6.590328692643546e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.118C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.180C>T
  hgvsp: ENST00000532544.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.180C>T
  hgvsp: ENST00000524704.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.372C>T
  hgvsp: ENST00000527737.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13177C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.180C>T
  hgvsp: ENST00000342935.3:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.303C>T
  hgvsp: ENST00000526958.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.180C>T
  hgvsp: ENST00000227155.4:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.123C>T
  hgvsp: ENST00000530601.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.352C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.180C>T
  hgvsp: ENST00000525813.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.237G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile60Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-44626654-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626654
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626654
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.183C>A
  hgvsp: ENST00000524704.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.183C>A
  hgvsp: ENST00000342935.3:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.306C>A
  hgvsp: ENST00000526958.1:c.306C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.183C>A
  hgvsp: ENST00000227155.4:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.375C>A
  hgvsp: ENST00000527737.1:c.375C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.126C>A
  hgvsp: ENST00000530601.1:c.126C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.234G>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.183C>A
  hgvsp: ENST00000532544.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13174C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.183C>A
  hgvsp: ENST00000525813.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.121C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.355C>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly61Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-44626654-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626654
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626654
    reference: chr 11
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.183C>G
  hgvsp: ENST00000227155.4:c.183C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.183C>G
  hgvsp: ENST00000342935.3:c.183C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.234G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.126C>G
  hgvsp: ENST00000530601.1:c.126C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.183C>G
  hgvsp: ENST00000532544.1:c.183C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.306C>G
  hgvsp: ENST00000526958.1:c.306C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.355C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.375C>G
  hgvsp: ENST00000527737.1:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.183C>G
  hgvsp: ENST00000525813.1:c.183C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.121C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13174C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.183C>G
  hgvsp: ENST00000524704.1:c.183C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15619
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly61Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-44626657-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626657
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626657
    reference: chr 11
allele count: 427
allele frequency: 3.517761813748105e-3
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.186G>A
  hgvsp: ENST00000524704.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.309G>A
  hgvsp: ENST00000526958.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.231C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.378G>A
  hgvsp: ENST00000527737.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.186G>A
  hgvsp: ENST00000227155.4:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.186G>A
  hgvsp: ENST00000525813.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.129G>A
  hgvsp: ENST00000530601.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.186G>A
  hgvsp: ENST00000532544.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.124G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.358G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.186G>A
  hgvsp: ENST00000342935.3:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13171G>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14575
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 15609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9344
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 243
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
hgvs: p.Val62Val
num of homozygotes: 9
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

11-44626669-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626669
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626669
    reference: chr 11
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.390T>C
  hgvsp: ENST00000527737.1:c.390T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.198T>C
  hgvsp: ENST00000525813.1:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.136T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.321T>C
  hgvsp: ENST00000526958.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.198T>C
  hgvsp: ENST00000524704.1:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.198T>C
  hgvsp: ENST00000342935.3:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.370T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.198T>C
  hgvsp: ENST00000532544.1:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.198T>C
  hgvsp: ENST00000227155.4:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.219A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.141T>C
  hgvsp: ENST00000530601.1:c.141T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13159T>C
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr66Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-44626670-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626670
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626670
    reference: chr 11
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.199A>G
  hgvsp: ENSP00000339686.3:p.Met67Val
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.199A>G
  hgvsp: ENSP00000431767.1:p.Met67Val
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.322A>G
  hgvsp: ENSP00000435682.1:p.Met108Val
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.199A>G
  hgvsp: ENSP00000227155.4:p.Met67Val
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13158A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.137A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000436403
  ensembl transcript: ENST00000524704
  gene symbol: CD82
  hgvsc: ENST00000524704.1:c.199A>G
  hgvsp: ENSP00000436403.1:p.Met67Val
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.142A>G
  hgvsp: ENSP00000433788.1:p.Met48Val
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.218T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.391A>G
  hgvsp: ENSP00000433151.1:p.Met131Val
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.371A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.199A>G
  hgvsp: ENSP00000433804.1:p.Met67Val
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met67Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-44626676-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626676
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626676
    reference: chr 11
allele count: 4
allele frequency: 3.296033224014898e-5
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.205A>C
  hgvsp: ENSP00000339686.3:p.Met69Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.205A>C
  hgvsp: ENSP00000433804.1:p.Met69Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.143A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.205A>C
  hgvsp: ENSP00000431767.1:p.Met69Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.212T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13152A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.397A>C
  hgvsp: ENSP00000433151.1:p.Met133Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.328A>C
  hgvsp: ENSP00000435682.1:p.Met110Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.377A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.148A>C
  hgvsp: ENSP00000433788.1:p.Met50Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.205A>C
  hgvsp: ENSP00000227155.4:p.Met69Leu
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Met69Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

11-44626676-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626676
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626676
    reference: chr 11
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.328A>T
  hgvsp: ENSP00000435682.1:p.Met110Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.205A>T
  hgvsp: ENSP00000431767.1:p.Met69Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.148A>T
  hgvsp: ENSP00000433788.1:p.Met50Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.377A>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.205A>T
  hgvsp: ENSP00000433804.1:p.Met69Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.205A>T
  hgvsp: ENSP00000339686.3:p.Met69Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.397A>T
  hgvsp: ENSP00000433151.1:p.Met133Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.143A>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13152A>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.205A>T
  hgvsp: ENSP00000227155.4:p.Met69Leu
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.212T>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met69Leu
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-44626684-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626684
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626684
    reference: chr 11
allele count: 20
allele frequency: 1.648342591524222e-4
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.405C>T
  hgvsp: ENST00000527737.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.213C>T
  hgvsp: ENST00000525813.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.385C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.336C>T
  hgvsp: ENST00000526958.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.156C>T
  hgvsp: ENST00000530601.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.213C>T
  hgvsp: ENST00000227155.4:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.204G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.213C>T
  hgvsp: ENST00000342935.3:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13144C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.213C>T
  hgvsp: ENST00000532544.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.151C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9393
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Phe71Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

11-44626692-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626692
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626692
    reference: chr 11
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.221G>T
  hgvsp: ENSP00000433804.1:p.Cys74Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.159G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.196C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.344G>T
  hgvsp: ENSP00000435682.1:p.Cys115Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13136G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.393G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.221G>T
  hgvsp: ENSP00000431767.1:p.Cys74Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.413G>T
  hgvsp: ENSP00000433151.1:p.Cys138Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.221G>T
  hgvsp: ENSP00000227155.4:p.Cys74Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.164G>T
  hgvsp: ENSP00000433788.1:p.Cys55Phe
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.221G>T
  hgvsp: ENSP00000339686.3:p.Cys74Phe
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys74Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

11-44626696-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626696
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626696
    reference: chr 11
allele count: 4
allele frequency: 3.299513321785036e-5
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.417C>G
  hgvsp: ENSP00000433151.1:p.Ile139Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.163C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.225C>G
  hgvsp: ENSP00000433804.1:p.Ile75Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.225C>G
  hgvsp: ENSP00000339686.3:p.Ile75Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.348C>G
  hgvsp: ENSP00000435682.1:p.Ile116Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.225C>G
  hgvsp: ENSP00000227155.4:p.Ile75Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.168C>G
  hgvsp: ENSP00000433788.1:p.Ile56Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.225C>G
  hgvsp: ENSP00000431767.1:p.Ile75Met
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.192G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13132C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.397C>G
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile75Met
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

11-44626697-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626697
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626697
    reference: chr 11
allele count: 3
allele frequency: 2.474594166556685e-5
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.191C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.226G>A
  hgvsp: ENSP00000227155.4:p.Gly76Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.226G>A
  hgvsp: ENSP00000433804.1:p.Gly76Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.226G>A
  hgvsp: ENSP00000431767.1:p.Gly76Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13131G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.226G>A
  hgvsp: ENSP00000339686.3:p.Gly76Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.418G>A
  hgvsp: ENSP00000433151.1:p.Gly140Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.164G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.169G>A
  hgvsp: ENSP00000433788.1:p.Gly57Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.349G>A
  hgvsp: ENSP00000435682.1:p.Gly117Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.398G>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly76Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

11-44626697-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626697
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626697
    reference: chr 11
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.349G>T
  hgvsp: ENSP00000435682.1:p.Gly117Cys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.226G>T
  hgvsp: ENSP00000227155.4:p.Gly76Cys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.226G>T
  hgvsp: ENSP00000433804.1:p.Gly76Cys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.226G>T
  hgvsp: ENSP00000339686.3:p.Gly76Cys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.169G>T
  hgvsp: ENSP00000433788.1:p.Gly57Cys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.226G>T
  hgvsp: ENSP00000431767.1:p.Gly76Cys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.418G>T
  hgvsp: ENSP00000433151.1:p.Gly140Cys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.191C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.164G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.398G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13131G>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly76Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD

11-44626702-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626702
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626702
    reference: chr 11
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.231C>T
  hgvsp: ENST00000525813.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.231C>T
  hgvsp: ENST00000227155.4:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.354C>T
  hgvsp: ENST00000526958.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.403C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13126C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.423C>T
  hgvsp: ENST00000527737.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.231C>T
  hgvsp: ENST00000532544.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.231C>T
  hgvsp: ENST00000342935.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.174C>T
  hgvsp: ENST00000530601.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.186G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.169C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala77Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-44626707-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626707
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626707
    reference: chr 11
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.236A>G
  hgvsp: ENSP00000433804.1:p.Asn79Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.236A>G
  hgvsp: ENSP00000431767.1:p.Asn79Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.428A>G
  hgvsp: ENSP00000433151.1:p.Asn143Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.181T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.236A>G
  hgvsp: ENSP00000339686.3:p.Asn79Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.359A>G
  hgvsp: ENSP00000435682.1:p.Asn120Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.236A>G
  hgvsp: ENSP00000227155.4:p.Asn79Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.179A>G
  hgvsp: ENSP00000433788.1:p.Asn60Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.174A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.408A>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13121A>G
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn79Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

11-44626709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626709
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626709
    reference: chr 11
allele count: 118
allele frequency: 9.74336955444727e-4
allele num: 121108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.361G>A
  hgvsp: ENSP00000435682.1:p.Glu121Lys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.410G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.181G>A
  hgvsp: ENSP00000433788.1:p.Glu61Lys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.430G>A
  hgvsp: ENSP00000433151.1:p.Glu144Lys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.179C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.176G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.238G>A
  hgvsp: ENSP00000227155.4:p.Glu80Lys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.238G>A
  hgvsp: ENSP00000431767.1:p.Glu80Lys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.238G>A
  hgvsp: ENSP00000339686.3:p.Glu80Lys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.238G>A
  hgvsp: ENSP00000433804.1:p.Glu80Lys
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13119G>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 14368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15411
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9325
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
hgvs: p.Glu80Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

11-44626715-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626715
    reference: chr 11
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.436C>G
  hgvsp: ENSP00000433151.1:p.Arg146Gly
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.173G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.244C>G
  hgvsp: ENSP00000433804.1:p.Arg82Gly
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.367C>G
  hgvsp: ENSP00000435682.1:p.Arg123Gly
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.244C>G
  hgvsp: ENSP00000339686.3:p.Arg82Gly
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.187C>G
  hgvsp: ENSP00000433788.1:p.Arg63Gly
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.244C>G
  hgvsp: ENSP00000227155.4:p.Arg82Gly
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.244C>G
  hgvsp: ENSP00000431767.1:p.Arg82Gly
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.416C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.182C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13113C>G
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg82Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

11-44626716-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626716
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626716
    reference: chr 11
allele count: 8
allele frequency: 6.612553933643021e-5
allele num: 120982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.368G>A
  hgvsp: ENSP00000435682.1:p.Arg123His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.245G>A
  hgvsp: ENSP00000227155.4:p.Arg82His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.437G>A
  hgvsp: ENSP00000433151.1:p.Arg146His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.417G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13112G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.245G>A
  hgvsp: ENSP00000339686.3:p.Arg82His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.188G>A
  hgvsp: ENSP00000433788.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.245G>A
  hgvsp: ENSP00000431767.1:p.Arg82His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.183G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.245G>A
  hgvsp: ENSP00000433804.1:p.Arg82His
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.172C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6734
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg82His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

11-44626721-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626721
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626721
    reference: chr 11
allele count: 2
allele frequency: 1.654478673769895e-5
allele num: 120884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.188C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.250C>T
  hgvsp: ENST00000227155.4:c.250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.422C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.250C>T
  hgvsp: ENST00000532544.1:c.250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.250C>T
  hgvsp: ENST00000342935.3:c.250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.167G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13107C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.442C>T
  hgvsp: ENST00000527737.1:c.442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.193C>T
  hgvsp: ENST00000530601.1:c.193C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.373C>T
  hgvsp: ENST00000526958.1:c.373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.250C>T
  hgvsp: ENST00000525813.1:c.250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu84Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

11-44626723-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626723
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626723
    reference: chr 11
allele count: 2
allele frequency: 1.654834599281802e-5
allele num: 120858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.252G>T
  hgvsp: ENST00000525813.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.165C>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.195G>T
  hgvsp: ENST00000530601.1:c.195G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13105G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.190G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.252G>T
  hgvsp: ENST00000532544.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.252G>T
  hgvsp: ENST00000342935.3:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.252G>T
  hgvsp: ENST00000227155.4:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.444G>T
  hgvsp: ENST00000527737.1:c.444G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.424G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.375G>T
  hgvsp: ENST00000526958.1:c.375G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu84Leu
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: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

11-44626729-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626729
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626729
    reference: chr 11
allele count: 41
allele frequency: 3.39595136335023e-4
allele num: 120732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.430G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.258G>T
  hgvsp: ENST00000532544.1:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.196G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.381G>T
  hgvsp: ENST00000526958.1:c.381G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13099G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.450G>T
  hgvsp: ENST00000527737.1:c.450G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.201G>T
  hgvsp: ENST00000530601.1:c.201G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.258G>T
  hgvsp: ENST00000342935.3:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.258G>T
  hgvsp: ENST00000525813.1:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.159C>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.258G>T
  hgvsp: ENST00000227155.4:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9234
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Gly86Gly
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-44626734-TGAGTACG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626734
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626727
    reference: chr 11
allele count: 1
allele frequency: 8.298341991270144e-6
allele num: 120506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+5_261+11delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.438_444delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.147_153delCGTACTC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+5_199+11delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+5_453+11delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+5_261+11delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+5_204+11delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+5_384+11delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+5_261+11delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+5_261+11delGTACGGA
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6680
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.261+5_261+11delGTACGGA
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: TGAGTACG
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

11-44626749-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626749
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626749
    reference: chr 11
allele count: 1
allele frequency: 8.333611120370679e-6
allele num: 119996
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.139G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+17C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+17C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+17C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+17C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+17C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+17C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13079C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+17C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.450C>G
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+17C>G
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

11-44626758-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626758
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626758
    reference: chr 11
allele count: 2
allele frequency: 1.670369318656355e-5
allele num: 119734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13070C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.130G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.459C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+26C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+26C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-44626762-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626762
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626762
    reference: chr 11
allele count: 1
allele frequency: 8.36456102783726e-6
allele num: 119552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+30C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.463C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+30C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+30C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+30C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13066C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+30C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.126G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+30C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+30C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+30C>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14514
  bin: 9.75e1
  variant carriers: 1
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: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/11-44626763-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626763
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626763
    reference: chr 11
allele count: 1
allele frequency: 8.36638053645232e-6
allele num: 119526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+31C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.464C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13065C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+31C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+31C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+31C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.125G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+31C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+31C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+31C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+31C>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-44626770-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626770
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626770
    reference: chr 11
allele count: 3
allele frequency: 2.51323637825883e-5
allele num: 119368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+38C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+38C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+38C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+38C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.471C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13058C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.118G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+38C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+38C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+38C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+38C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

11-44626772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626772
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626772
    reference: chr 11
allele count: 1
allele frequency: 8.389120987902887e-6
allele num: 119202
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+40C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.116G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+40C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+40C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.473C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+40C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+40C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+40C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+40C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+40C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13056C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-44626779-AGCCGAGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626779
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626772
    reference: chr 11
allele count: 1
allele frequency: 8.406610958858046e-6
allele num: 118954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+50_261+56delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+50_261+56delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.483_489delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+50_204+56delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+50_453+56delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+50_199+56delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.102_108delACTCGGC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+50_261+56delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+50_261+56delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+50_384+56delCGAGTGC
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8589
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: AGCCGAGT
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

11-44626782-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626782
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626782
    reference: chr 11
allele count: 3
allele frequency: 2.525635197252109e-5
allele num: 118782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+50C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+50C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+50C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+50C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13046C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.106G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.483C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+50C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+50C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+50C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+50C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10363
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8826
  bin: 6.25e1
  variant carriers: 0
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: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

11-44626783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626783
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626783
    reference: chr 11
allele count: 1
allele frequency: 8.408307407718826e-6
allele num: 118930
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+51G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+51G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+51G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.105C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.484G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+51G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+51G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+51G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+51G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+51G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13045G>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1932
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9498
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-44626783-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626783
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626783
    reference: chr 11
allele count: 1
allele frequency: 8.408307407718826e-6
allele num: 118930
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.105C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.484G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.199+51G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.453+51G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.261+51G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-13045G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.261+51G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.384+51G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.204+51G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.261+51G>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+51G>C
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14499
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9498
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

11-44626863-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626863
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626863
    reference: chr 11
allele count: 2
allele frequency: 1.65461555007694e-5
allele num: 120874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12965C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.564C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.454-42C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+131C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.262-42C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.262-42C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.25G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.262-42C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.385-42C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.200-42C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.205-42C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-44626869-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626869
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626869
    reference: chr 11
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.570C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12959C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.205-36C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.385-36C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+137C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.262-36C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.262-36C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.19G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.262-36C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.200-36C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.454-36C>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-44626869-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626869
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626869
    reference: chr 11
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12959C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.262-36C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.262-36C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.454-36C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.19G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.570C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.262-36C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.385-36C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.200-36C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+137C>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.205-36C>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/11-44626874-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626874
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626874
    reference: chr 11
allele count: 2
allele frequency: 1.651554938975045e-5
allele num: 121098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12954A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.454-31A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254693
  ensembl transcript: ENST00000533814
  gene symbol: RP11-58K22.5
  hgvsc: ENST00000533814.1:n.14T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.575A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.385-31A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.262-31A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.205-31A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.200-31A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.262-31A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.262-31A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+142A>C
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/11-44626937-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626937
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626937
    reference: chr 11
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.294C>A
  hgvsp: ENST00000227155.4:c.294C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.237C>A
  hgvsp: ENST00000530601.1:c.237C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.638C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.232C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.294C>A
  hgvsp: ENST00000532544.1:c.294C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12891C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.486C>A
  hgvsp: ENST00000527737.1:c.486C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.294C>A
  hgvsp: ENST00000525813.1:c.294C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+205C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.417C>A
  hgvsp: ENST00000526958.1:c.417C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36742
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala98Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/11-44626939-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626939
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626939
    reference: chr 11
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12889A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.296A>C
  hgvsp: ENSP00000433804.1:p.Gln99Pro
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.239A>C
  hgvsp: ENSP00000433788.1:p.Gln80Pro
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.488A>C
  hgvsp: ENSP00000433151.1:p.Gln163Pro
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.640A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.296A>C
  hgvsp: ENSP00000431767.1:p.Gln99Pro
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.296A>C
  hgvsp: ENSP00000227155.4:p.Gln99Pro
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.419A>C
  hgvsp: ENSP00000435682.1:p.Gln140Pro
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+207A>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.234A>C
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln99Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

11-44626947-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626947
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626947
    reference: chr 11
allele count: 5
allele frequency: 4.123371268349002e-5
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.427G>T
  hgvsp: ENSP00000435682.1:p.Ala143Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.648G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+215G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.304G>T
  hgvsp: ENSP00000431767.1:p.Ala102Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.247G>T
  hgvsp: ENSP00000433788.1:p.Ala83Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.304G>T
  hgvsp: ENSP00000227155.4:p.Ala102Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.496G>T
  hgvsp: ENSP00000433151.1:p.Ala166Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.304G>T
  hgvsp: ENSP00000433804.1:p.Ala102Ser
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12881G>T
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.242G>T
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9423
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36680
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala102Ser
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-44626948-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626948
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626948
    reference: chr 11
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.243C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.305C>A
  hgvsp: ENSP00000431767.1:p.Ala102Asp
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.497C>A
  hgvsp: ENSP00000433151.1:p.Ala166Asp
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.248C>A
  hgvsp: ENSP00000433788.1:p.Ala83Asp
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.428C>A
  hgvsp: ENSP00000435682.1:p.Ala143Asp
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.305C>A
  hgvsp: ENSP00000433804.1:p.Ala102Asp
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.305C>A
  hgvsp: ENSP00000227155.4:p.Ala102Asp
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+216C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.649C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12880C>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9418
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala102Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

11-44626950-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626950
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626950
    reference: chr 11
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.307G>A
  hgvsp: ENSP00000433804.1:p.Gly103Arg
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.499G>A
  hgvsp: ENSP00000433151.1:p.Gly167Arg
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.245G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.250G>A
  hgvsp: ENSP00000433788.1:p.Gly84Arg
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.651G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+218G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.430G>A
  hgvsp: ENSP00000435682.1:p.Gly144Arg
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12878G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.307G>A
  hgvsp: ENSP00000227155.4:p.Gly103Arg
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.307G>A
  hgvsp: ENSP00000431767.1:p.Gly103Arg
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly103Arg
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-44626953-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626953
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626953
    reference: chr 11
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12875G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.433G>A
  hgvsp: ENSP00000435682.1:p.Ala145Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000431767
  ensembl transcript: ENST00000532544
  gene symbol: CD82
  hgvsc: ENST00000532544.1:c.310G>A
  hgvsp: ENSP00000431767.1:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.253G>A
  hgvsp: ENSP00000433788.1:p.Ala85Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.310G>A
  hgvsp: ENSP00000227155.4:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.248G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.502G>A
  hgvsp: ENSP00000433151.1:p.Ala168Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.654G>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433804
  ensembl transcript: ENST00000525813
  gene symbol: CD82
  hgvsc: ENST00000525813.1:c.310G>A
  hgvsp: ENSP00000433804.1:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+221G>A
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36651
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala104Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-44626972-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626972
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626972
    reference: chr 11
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.521T>C
  hgvsp: ENSP00000433151.1:p.Met174Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.272T>C
  hgvsp: ENSP00000433788.1:p.Met91Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.452T>C
  hgvsp: ENSP00000435682.1:p.Met151Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12856T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.267T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.673T>C
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.329T>C
  hgvsp: ENSP00000227155.4:p.Met110Thr
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+240T>C
  variant of: http://identifiers.org/hgnc/6210
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27268
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met110Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/11-44626985-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44626985
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44626985
    reference: chr 11
allele count: 1
allele frequency: 8.286789200656313e-6
allele num: 120674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000435682
  ensembl transcript: ENST00000526958
  gene symbol: CD82
  hgvsc: ENST00000526958.1:c.459+6C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000525898
  gene symbol: CD82
  hgvsc: ENST00000525898.1:n.680+6C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000529277
  gene symbol: CD82
  hgvsc: ENST00000529277.1:n.125-12843C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433788
  ensembl transcript: ENST00000530601
  gene symbol: CD82
  hgvsc: ENST00000530601.1:c.279+6C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl transcript: ENST00000530931
  gene symbol: CD82
  hgvsc: ENST00000530931.1:n.274+6C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000227155
  ensembl transcript: ENST00000227155
  gene symbol: CD82
  hgvsc: ENST00000227155.4:c.336+6C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000339686
  ensembl transcript: ENST00000342935
  gene symbol: CD82
  hgvsc: ENST00000342935.3:c.261+253C>A
  variant of: http://identifiers.org/hgnc/6210
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085117
  ensembl protein: ENSP00000433151
  ensembl transcript: ENST00000527737
  gene symbol: CD82
  hgvsc: ENST00000527737.1:c.534C>A
  hgvsp: ENSP00000433151.1:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/6210
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser178Arg
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 3618
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7932
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15262
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2394
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4761
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3850
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17141
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5584
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.102e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.082e0

DP
type: SiteQuality
SIO_000300: 2.244855e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.44e-1

GenotypeDepth
all individuals: 6515
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7917
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5580
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4757
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3848
bin: 7.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17081
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15262
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3618
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.498950146979423e-5
allele num: 66676
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817961459217065e-4
allele num: 16502
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

FS
type: SiteQuality
SIO_000300: 4.499e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

DP
type: SiteQuality
SIO_000300: 2.244414e6

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16839
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4737
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15255
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3824
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7854
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.911e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-2

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.381e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e-1

DP
type: SiteQuality
SIO_000300: 2.240535e6

FS
type: SiteQuality
SIO_000300: 1.323e0

VQSLOD
type: SiteQuality
SIO_000300: 9.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-1

GenotypeQuality
all individuals: 268
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15252
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 5564
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3822
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16646
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3613
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4734
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2387
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.271e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.264e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.815e1

DP
type: SiteQuality
SIO_000300: 2.23856e6

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16018
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7701
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2375
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15234
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 329
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5505
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4702
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 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: 11564
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.939e0

QD
type: SiteQuality
SIO_000300: 1.771e1

VQSLOD
type: SiteQuality
SIO_000300: -6.68e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 2.228722e6

GenotypeQuality
all individuals: 15232
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 422
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15709
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7597
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4698
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3769
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.013339742819372e-5
allele num: 66568
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

FS
type: SiteQuality
SIO_000300: 2.517e0

DP
type: SiteQuality
SIO_000300: 2.225495e6

MQ
type: SiteQuality
SIO_000300: 5.93e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.287e0

QD
type: SiteQuality
SIO_000300: 1.367e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
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GenotypeQuality
all individuals: 7
bin: 1.25e1
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GenotypeQuality
all individuals: 482
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3766
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15227
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.761e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.91e-1

FS
type: SiteQuality
SIO_000300: 5.448e0

DP
type: SiteQuality
SIO_000300: 2.224945e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.141e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 16251
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

FS
type: SiteQuality
SIO_000300: 2.901e0

VQSLOD
type: SiteQuality
SIO_000300: 1.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.008e0

MQRankSum
type: SiteQuality
SIO_000300: -1.344e0

QD
type: SiteQuality
SIO_000300: 1.181e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.317617e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

GenotypeDepth
all individuals: 279
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16371
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3460
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.901e0

VQSLOD
type: SiteQuality
SIO_000300: 1.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.344e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.008e0

QD
type: SiteQuality
SIO_000300: 1.181e1

DP
type: SiteQuality
SIO_000300: 2.317617e6

GenotypeDepth
all individuals: 3356
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16388
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 5220
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 8318
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2317
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 4483
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3459
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16369
bin: 9.75e1
variant carriers: 3

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: 10396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

DP
type: SiteQuality
SIO_000300: 2.318674e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

GenotypeDepth
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8325
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variant carriers: 0

GenotypeQuality
all individuals: 4481
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3853
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3457
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16364
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998860433035446e-5
allele num: 66692
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.606e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 1.4129e1

DP
type: SiteQuality
SIO_000300: 2.31916e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.103e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 22
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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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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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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49829064955317e-5
allele num: 66692
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.35e-1

VQSLOD
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 1.868e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.31924e6

QD
type: SiteQuality
SIO_000300: 1.106e1

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
all individuals: 32
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16359
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

FS
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ClippingRankSum
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SIO_000300: 9.71e-1

VQSLOD
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DP
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ReadPosRankSum
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MQ
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SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

QD
type: SiteQuality
SIO_000300: 1.407e1

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
all individuals: 39
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8652
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
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SIO_000300: 1.626e1

MQ
type: SiteQuality
SIO_000300: 5.882e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-2

FS
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
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SIO_000300: -1.564e0

MQRankSum
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SIO_000300: -3.76e-1

BaseQRankSum
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SIO_000300: 9.17e-1

VQSLOD
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SIO_000300: 3.19e0

DP
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SIO_000300: 2.319309e6

GenotypeDepth
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variant carriers: 17

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: 1654

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele count: 101
allele frequency: 8.723441008809812e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1149
allele frequency: 1.722690335542295e-2
allele num: 66698
num of homozygotes: 16

African
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allele count: 18
allele frequency: 1.730436454527975e-3
allele num: 10402
num of homozygotes: 0

European (Finnish)
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allele count: 62
allele frequency: 9.37405503477472e-3
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 23
allele frequency: 2.533039647577092e-2
allele num: 908
num of homozygotes: 1

South Asian
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allele count: 321
allele frequency: 1.944040697674419e-2
allele num: 16512
num of homozygotes: 4

East Asian
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allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-2

MQ
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SIO_000300: 5.961e1

ReadPosRankSum
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SIO_000300: 6.870000000000001e-1

VQSLOD
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MQRankSum
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ClippingRankSum
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SIO_000300: -4.84e-1

BaseQRankSum
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DP
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SIO_000300: 2.389713e6

FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.238e1

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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bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 9
allele frequency: 1.349082623815805e-4
allele num: 66712
num of homozygotes: 0

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

DP
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SIO_000300: 2.218377e6

InbreedingCoeff
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MQ
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SIO_000300: 5.946e1

ReadPosRankSum
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SIO_000300: 6.11e-1

MQRankSum
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SIO_000300: -9.9e-2

BaseQRankSum
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FS
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SIO_000300: 1.14e0

ClippingRankSum
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SIO_000300: -1.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.48e-1

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

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
all individuals: 11
bin: 4.25e1
variant carriers: 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: 8652
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

South Asian
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allele count: 0
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num of homozygotes: 0

MQRankSum
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SIO_000300: -3.48e-1

BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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SIO_000300: 2.309e0

MQ
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SIO_000300: 5.941e1

VQSLOD
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SIO_000300: -2.901e0

DP
type: SiteQuality
SIO_000300: 2.217572e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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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variant carriers: 2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
num of homozygotes: 0

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

Latino
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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
allele num: 10400
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

South Asian
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num of homozygotes: 0

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

InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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QD
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ReadPosRankSum
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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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
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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Latino
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num of homozygotes: 0

FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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MQ
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BaseQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

European (Finnish)
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allele num: 6614
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African
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allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
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Other
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East Asian
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Latino
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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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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variant carriers: 0

African
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allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
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East Asian
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Latino
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African
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South Asian
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Other
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
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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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East Asian
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Latino
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African
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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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Other
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South Asian
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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FS
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QD
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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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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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

European (Non-Finnish)
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Latino
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allele frequency: 1.727712508638563e-3
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African
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South Asian
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Other
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East Asian
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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VQSLOD
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ClippingRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 10404
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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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European (Non-Finnish)
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Other
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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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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Other
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European (Finnish)
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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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European (Non-Finnish)
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MQ
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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Other
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South Asian
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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MQ
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FS
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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South Asian
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.003662233962717e-5
allele num: 66626
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

ReadPosRankSum
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SIO_000300: -7.09e-1

FS
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InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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MQRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.185613e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.03e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

GenotypeQuality
all individuals: 2370
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.50220608097968e-5
allele num: 66634
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

MQRankSum
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MQ
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ReadPosRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.326e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

FS
type: SiteQuality
SIO_000300: 2.712e0

DP
type: SiteQuality
SIO_000300: 2.184852e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
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

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: 8.139999999999999e-1

DP
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SIO_000300: 2.184852e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

FS
type: SiteQuality
SIO_000300: 2.712e0

QD
type: SiteQuality
SIO_000300: 1.293e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.551e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

MQ
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

QD
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SIO_000300: 1.596e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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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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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: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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VQSLOD
type: SiteQuality
SIO_000300: 9.77e-1

DP
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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SIO_000300: 5.18e-1

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-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

Latino
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allele count: 3
allele frequency: 2.594706798131811e-4
allele num: 11562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.029385034837928e-4
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
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allele count: 105
allele frequency: 1.577239680346092e-3
allele num: 66572
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.887947631882942e-4
allele num: 10388
num of homozygotes: 0

East Asian
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allele num: 8650
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South Asian
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allele frequency: 3.042472921990994e-4
allele num: 16434
num of homozygotes: 0

Other
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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DP
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InbreedingCoeff
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SIO_000300: -1.3e-3

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

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
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South Asian
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allele count: 1
allele frequency: 6.1020258725897e-5
allele num: 16388
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Latino
type: Population
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allele frequency: 0.0e0
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Other
type: Population
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.202754307363863e-4
allele num: 66514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.486e0

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

QD
type: SiteQuality
SIO_000300: 1.335e1

FS
type: SiteQuality
SIO_000300: 4.821e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-1

DP
type: SiteQuality
SIO_000300: 2.166652e6

GenotypeQuality
all individuals: 3538
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3858
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2343
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.516070345664039e-4
allele num: 6596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66484
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.086e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

FS
type: SiteQuality
SIO_000300: 9.215999999999999e0

QD
type: SiteQuality
SIO_000300: 1.25e1

DP
type: SiteQuality
SIO_000300: 2.160147e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 706
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008514094888535e-5
allele num: 66478
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 5.03e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

VQSLOD
type: SiteQuality
SIO_000300: 8.62e-1

QD
type: SiteQuality
SIO_000300: 1.26e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.158549e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.35e0

GenotypeQuality
all individuals: 3814
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 87
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 14638
bin: 9.75e1
variant carriers: 41

GenotypeQuality
all individuals: 16303
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 39
allele frequency: 3.757949508575833e-3
allele num: 10378
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: 11550
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66428
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.314814814814815e-4
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.532e0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

FS
type: SiteQuality
SIO_000300: 6.0e-1

DP
type: SiteQuality
SIO_000300: 2.149985e6

VQSLOD
type: SiteQuality
SIO_000300: 4.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

QD
type: SiteQuality
SIO_000300: 1.326e1

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
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GenotypeQuality
all individuals: 161
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GenotypeQuality
all individuals: 14592
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variant carriers: 1

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 507
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GenotypeQuality
all individuals: 4548
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7981
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3528
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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: 1218
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variant carriers: 0

GenotypeQuality
all individuals: 180
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variant carriers: 0

GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 8.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507431637975218e-5
allele num: 66338
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.395e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

DP
type: SiteQuality
SIO_000300: 2.135526e6

FS
type: SiteQuality
SIO_000300: 9.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 4.989e1

QD
type: SiteQuality
SIO_000300: 7.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

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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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
all individuals: 13175
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513042425709617e-5
allele num: 66092
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15968
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 2.092559e6

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.612e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 1.485e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.313e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029843963035904e-5
allele num: 66010
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.142e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.303e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3466
bin: 7.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516944267467613e-5
allele num: 65922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15738
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.199e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.344e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.44e0

DP
type: SiteQuality
SIO_000300: 2.067006e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3446
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 426
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GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 12972
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GenotypeQuality
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GenotypeQuality
all individuals: 317
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GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 1492
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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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variant carriers: 0

GenotypeQuality
all individuals: 14512
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7085
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51666818333485e-5
allele num: 65934
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e-1

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

FS
type: SiteQuality
SIO_000300: 1.485e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 2.066495e6

GenotypeQuality
all individuals: 3374
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.915708812260536e-4
allele num: 15660
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

DP
type: SiteQuality
SIO_000300: 2.051934e6

FS
type: SiteQuality
SIO_000300: 1.18e1

VQSLOD
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SIO_000300: -1.524e0

QD
type: SiteQuality
SIO_000300: 1.304e1

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e0

GenotypeQuality
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bin: 9.75e1
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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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.411078343377356e-5
allele num: 15598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65786
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.353e-1

DP
type: SiteQuality
SIO_000300: 2.043128e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.539e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

GenotypeQuality
all individuals: 1945
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4668
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variant carriers: 0

GenotypeQuality
all individuals: 3461
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15542
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523182842868458e-5
allele num: 65652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.129e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e-1

MQ
type: SiteQuality
SIO_000300: 5.316e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 4.605e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

QD
type: SiteQuality
SIO_000300: 5.95e0

DP
type: SiteQuality
SIO_000300: 2.025183e6

GenotypeQuality
all individuals: 3059
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1974
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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: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4365
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variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.94149624644059e-4
allele num: 15452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65598
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.769e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.56e-1

QD
type: SiteQuality
SIO_000300: 1.516e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

DP
type: SiteQuality
SIO_000300: 2.02376e6

GenotypeQuality
all individuals: 356
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3473
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variant carriers: 0

GenotypeQuality
all individuals: 4710
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523368472366096e-5
allele num: 65644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15548
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.624e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.112e0

FS
type: SiteQuality
SIO_000300: 2.527e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 5.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

DP
type: SiteQuality
SIO_000300: 2.024705e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.83e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.724480893386844e-5
allele num: 11462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15548
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.93e-1

FS
type: SiteQuality
SIO_000300: 2.527e0

DP
type: SiteQuality
SIO_000300: 2.024705e6

QD
type: SiteQuality
SIO_000300: 1.624e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.83e-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
all individuals: 1122
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GenotypeQuality
all individuals: 3065
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.087909411907951e-5
allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505343971097396e-5
allele num: 66430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
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: 11550
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 2.592e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.66e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.11e-2

DP
type: SiteQuality
SIO_000300: 1.777403e6

FS
type: SiteQuality
SIO_000300: 9.412000000000001e0

QD
type: SiteQuality
SIO_000300: 1.369e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.528e0

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

GenotypeQuality
all individuals: 3576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

BaseQRankSum
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SIO_000300: -1.528e0

QD
type: SiteQuality
SIO_000300: 1.369e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

FS
type: SiteQuality
SIO_000300: 9.412000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

DP
type: SiteQuality
SIO_000300: 1.777403e6

VQSLOD
type: SiteQuality
SIO_000300: -3.11e-2

GenotypeQuality
all individuals: 251
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
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: 2
allele frequency: 1.730403183941858e-4
allele num: 11558
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

FS
type: SiteQuality
SIO_000300: 4.211e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

QD
type: SiteQuality
SIO_000300: 1.624e1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1

DP
type: SiteQuality
SIO_000300: 1.782905e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.503e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.243e0

QD
type: SiteQuality
SIO_000300: 5.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

DP
type: SiteQuality
SIO_000300: 1.793408e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.466e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: -3.99e-1

DP
type: SiteQuality
SIO_000300: 1.793293e6

QD
type: SiteQuality
SIO_000300: 6.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3543
bin: 9.75e1
variant carriers: 5

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.501425270801452e-5
allele num: 66654
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.267e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.09e0

DP
type: SiteQuality
SIO_000300: 1.792772e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -9.0e-1

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.824e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e0

QD
type: SiteQuality
SIO_000300: 1.036e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.927e0

DP
type: SiteQuality
SIO_000300: 1.792386e6

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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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
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: 11566
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: -1.08e0

QD
type: SiteQuality
SIO_000300: 1.574e1

DP
type: SiteQuality
SIO_000300: 1.792454e6

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e-1

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3546
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9407
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 2142
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.496e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 2.425e1

FS
type: SiteQuality
SIO_000300: 1.487e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

DP
type: SiteQuality
SIO_000300: 1.791818e6

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1103
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9353
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3011
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36282
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 901
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2133
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.675e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

DP
type: SiteQuality
SIO_000300: 1.786394e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.25e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.94e-1

QD
type: SiteQuality
SIO_000300: 1.151e1