7-80141257-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80141257
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80141257
    reference: chr 7
allele count: 1
allele frequency: 1.166561676115816e-5
allele num: 85722
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-261+24160T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000214415
  ensembl protein: ENSP00000381339
  ensembl transcript: ENST00000398291
  gene symbol: GNAT3
  hgvsc: ENST00000398291.3:c.-15A>G
  variant of: http://identifiers.org/hgnc/22800
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27410
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3374
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10360
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4293
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 12492
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

7-80141259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80141259
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80141259
    reference: chr 7
allele count: 1
allele frequency: 1.179078432297316e-5
allele num: 84812
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000214415
  ensembl protein: ENSP00000381339
  ensembl transcript: ENST00000398291
  gene symbol: GNAT3
  hgvsc: ENST00000398291.3:c.-17G>A
  variant of: http://identifiers.org/hgnc/22800
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-261+24162C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3903
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4293
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2958
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3451
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 420
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genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9911
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 646
  num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

7-80141268-TTA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80141268
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80141266
    reference: chr 7
allele count: 20
allele frequency: 2.541619011310205e-4
allele num: 78690
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-261+24175_-261+24176delAT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000214415
  ensembl protein: ENSP00000381339
  ensembl transcript: ENST00000398291
  gene symbol: GNAT3
  hgvsc: ENST00000398291.3:c.-28_-27delTA
  variant of: http://identifiers.org/hgnc/22800
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20674
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16307
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25809
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4267
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 369
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 419
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 143
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6529
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 1
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11810
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: TTA
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

7-80141279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80141279
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80141279
    reference: chr 7
allele count: 2
allele frequency: 2.816980760021409e-5
allele num: 70998
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000214415
  ensembl protein: ENSP00000381339
  ensembl transcript: ENST00000398291
  gene symbol: GNAT3
  hgvsc: ENST00000398291.3:c.-37C>T
  variant of: http://identifiers.org/hgnc/22800
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-261+24182G>A
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17956
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.25e1
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
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genotype quality: GenotypeQuality
  all individuals: 2630
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 418
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 21894
  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4295
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 845
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 2
  allele frequency: 2.893518518518518e-4
  allele num: 6912
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

7-80141279-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80141279
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80141279
    reference: chr 7
allele count: 1
allele frequency: 1.408490380010705e-5
allele num: 70998
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000214415
  ensembl protein: ENSP00000381339
  ensembl transcript: ENST00000398291
  gene symbol: GNAT3
  hgvsc: ENST00000398291.3:c.-37C>A
  variant of: http://identifiers.org/hgnc/22800
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-261+24182G>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17956
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6798
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3213
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4438
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2630
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4295
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4564
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-80276006-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276006
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276006
    reference: chr 7
allele count: 5
allele frequency: 4.120516877637131e-5
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.363A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9850A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.460A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.237A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-51A>G
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

7-80276012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276012
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276012
    reference: chr 7
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9844C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.243C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.466C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.369C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-45C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

7-80276013-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276013
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276013
    reference: chr 7
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.467A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.370A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9843A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.244A>G
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6922
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

7-80276015-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276015
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276015
    reference: chr 7
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.469G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9841G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.246G>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.372G>C
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/7-80276017-AAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276017
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276015
    reference: chr 7
allele count: 4
allele frequency: 3.29614186594591e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.473_474delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9837_-108-9836delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.250_251delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.376_377delCA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-38_-37delCA
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: AAC
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-80276030-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276030
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276030
    reference: chr 7
allele count: 9
allele frequency: 7.416563658838072e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9826C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.261C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.387C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.484C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-27C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-80276038-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276038
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276039
    reference: chr 7
allele count: 57
allele frequency: 4.69676994067238e-4
allele num: 121360
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.396dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.270dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9817dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-18dupA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.493dupA
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/7-80276040-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276040
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276040
    reference: chr 7
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.397C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.494C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9816C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-17C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.271C>A
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

7-80276040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276040
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276040
    reference: chr 7
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000526804
  gene symbol: CD36
  hgvsc: ENST00000526804.1:n.494C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.397C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9816C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.271C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

7-80276045-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276045
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276045
    reference: chr 7
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.276T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9811T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-12T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.402T>C
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-80276050-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276050
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276050
    reference: chr 7
allele count: 4
allele frequency: 3.295544423938835e-5
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.281A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.407A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9806A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.-7A>G
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

7-80276057-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276057
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276057
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.1A>T
  hgvsp: ENSP00000399421.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.1A>T
  hgvsp: ENSP00000392298.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.1A>T
  hgvsp: ENSP00000439543.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.1A>T
  hgvsp: ENSP00000409762.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.1A>T
  hgvsp: ENSP00000441956.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.1A>T
  hgvsp: ENSP00000407690.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.1A>T
  hgvsp: ENSP00000401863.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9799A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.1A>T
  hgvsp: ENSP00000416388.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.1A>T
  hgvsp: ENSP00000378268.3:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.1A>T
  hgvsp: ENSP00000308165.7:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.1A>T
  hgvsp: ENSP00000415743.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.1A>T
  hgvsp: ENSP00000411411.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.1A>T
  hgvsp: ENSP00000433659.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.1A>T
  hgvsp: ENSP00000398760.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.1A>T
  hgvsp: ENSP00000396258.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.1A>T
  hgvsp: ENSP00000410371.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.414A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.288A>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

7-80276058-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276058
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276058
    reference: chr 7
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.2T>C
  hgvsp: ENSP00000308165.7:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.2T>C
  hgvsp: ENSP00000407690.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.2T>C
  hgvsp: ENSP00000398760.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.2T>C
  hgvsp: ENSP00000439543.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.2T>C
  hgvsp: ENSP00000392298.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.2T>C
  hgvsp: ENSP00000399421.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.2T>C
  hgvsp: ENSP00000378268.3:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.2T>C
  hgvsp: ENSP00000433659.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.2T>C
  hgvsp: ENSP00000415743.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.2T>C
  hgvsp: ENSP00000441956.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.2T>C
  hgvsp: ENSP00000411411.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.415T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.2T>C
  hgvsp: ENSP00000410371.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.289T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.2T>C
  hgvsp: ENSP00000409762.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.2T>C
  hgvsp: ENSP00000396258.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.2T>C
  hgvsp: ENSP00000416388.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.2T>C
  hgvsp: ENSP00000401863.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9798T>C
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-80276059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276059
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276059
    reference: chr 7
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.3G>A
  hgvsp: ENSP00000407690.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.3G>A
  hgvsp: ENSP00000410371.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.3G>A
  hgvsp: ENSP00000433659.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.3G>A
  hgvsp: ENSP00000411411.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.3G>A
  hgvsp: ENSP00000308165.7:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.3G>A
  hgvsp: ENSP00000392298.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.3G>A
  hgvsp: ENSP00000378268.3:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.3G>A
  hgvsp: ENSP00000441956.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.3G>A
  hgvsp: ENSP00000398760.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9797G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.3G>A
  hgvsp: ENSP00000439543.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.3G>A
  hgvsp: ENSP00000401863.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.416G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.3G>A
  hgvsp: ENSP00000396258.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.3G>A
  hgvsp: ENSP00000416388.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.290G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.3G>A
  hgvsp: ENSP00000399421.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.3G>A
  hgvsp: ENSP00000415743.2:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.3G>A
  hgvsp: ENSP00000409762.1:p.Met1?
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD

7-80276061-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276061
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276061
    reference: chr 7
allele count: 24
allele frequency: 1.977326654363301e-4
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.5G>T
  hgvsp: ENSP00000441956.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.5G>T
  hgvsp: ENSP00000439543.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.5G>T
  hgvsp: ENSP00000308165.7:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.5G>T
  hgvsp: ENSP00000399421.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.5G>T
  hgvsp: ENSP00000411411.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.5G>T
  hgvsp: ENSP00000398760.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.418G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.5G>T
  hgvsp: ENSP00000409762.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.292G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.5G>T
  hgvsp: ENSP00000410371.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.5G>T
  hgvsp: ENSP00000407690.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.5G>T
  hgvsp: ENSP00000378268.3:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.5G>T
  hgvsp: ENSP00000433659.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.5G>T
  hgvsp: ENSP00000401863.2:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.5G>T
  hgvsp: ENSP00000392298.2:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.5G>T
  hgvsp: ENSP00000416388.1:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.5G>T
  hgvsp: ENSP00000396258.2:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.5G>T
  hgvsp: ENSP00000415743.2:p.Gly2Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9795G>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly2Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

7-80276068-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276068
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276068
    reference: chr 7
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.12C>G
  hgvsp: ENSP00000441956.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.12C>G
  hgvsp: ENSP00000407690.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.12C>G
  hgvsp: ENSP00000415743.2:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.12C>G
  hgvsp: ENSP00000392298.2:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.12C>G
  hgvsp: ENSP00000409762.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.12C>G
  hgvsp: ENSP00000433659.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9788C>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.12C>G
  hgvsp: ENSP00000398760.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.12C>G
  hgvsp: ENSP00000401863.2:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.12C>G
  hgvsp: ENSP00000439543.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.12C>G
  hgvsp: ENSP00000308165.7:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.12C>G
  hgvsp: ENSP00000411411.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.425C>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.12C>G
  hgvsp: ENSP00000410371.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.12C>G
  hgvsp: ENSP00000399421.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.12C>G
  hgvsp: ENSP00000396258.2:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.299C>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.12C>G
  hgvsp: ENSP00000378268.3:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.12C>G
  hgvsp: ENSP00000416388.1:p.Asp4Glu
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp4Glu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

7-80276069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276069
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276069
    reference: chr 7
allele count: 8
allele frequency: 6.59098024353672e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.13C>T
  hgvsp: ENSP00000392298.2:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.426C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.13C>T
  hgvsp: ENSP00000441956.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.13C>T
  hgvsp: ENSP00000415743.2:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.13C>T
  hgvsp: ENSP00000416388.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.13C>T
  hgvsp: ENSP00000411411.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.13C>T
  hgvsp: ENSP00000409762.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.13C>T
  hgvsp: ENSP00000407690.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.13C>T
  hgvsp: ENSP00000398760.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.13C>T
  hgvsp: ENSP00000399421.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.13C>T
  hgvsp: ENSP00000439543.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.13C>T
  hgvsp: ENSP00000378268.3:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.13C>T
  hgvsp: ENSP00000401863.2:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.13C>T
  hgvsp: ENSP00000410371.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.13C>T
  hgvsp: ENSP00000308165.7:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.13C>T
  hgvsp: ENSP00000396258.2:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.13C>T
  hgvsp: ENSP00000433659.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9787C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.300C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg5Trp
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

7-80276070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276070
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276070
    reference: chr 7
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.14G>A
  hgvsp: ENSP00000416388.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.14G>A
  hgvsp: ENSP00000399421.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.14G>A
  hgvsp: ENSP00000378268.3:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.14G>A
  hgvsp: ENSP00000401863.2:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.14G>A
  hgvsp: ENSP00000411411.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.14G>A
  hgvsp: ENSP00000439543.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.14G>A
  hgvsp: ENSP00000433659.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.14G>A
  hgvsp: ENSP00000392298.2:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.14G>A
  hgvsp: ENSP00000441956.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.14G>A
  hgvsp: ENSP00000308165.7:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.14G>A
  hgvsp: ENSP00000398760.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.301G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.14G>A
  hgvsp: ENSP00000410371.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.14G>A
  hgvsp: ENSP00000396258.2:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9786G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.427G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.14G>A
  hgvsp: ENSP00000415743.2:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.14G>A
  hgvsp: ENSP00000409762.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.14G>A
  hgvsp: ENSP00000407690.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg5Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

7-80276070-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276070
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276070
    reference: chr 7
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.14G>T
  hgvsp: ENSP00000378268.3:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.14G>T
  hgvsp: ENSP00000308165.7:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.14G>T
  hgvsp: ENSP00000396258.2:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.14G>T
  hgvsp: ENSP00000398760.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.14G>T
  hgvsp: ENSP00000411411.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.14G>T
  hgvsp: ENSP00000441956.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.14G>T
  hgvsp: ENSP00000399421.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.14G>T
  hgvsp: ENSP00000416388.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.14G>T
  hgvsp: ENSP00000433659.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.14G>T
  hgvsp: ENSP00000439543.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.14G>T
  hgvsp: ENSP00000409762.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.14G>T
  hgvsp: ENSP00000392298.2:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.14G>T
  hgvsp: ENSP00000401863.2:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.301G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.14G>T
  hgvsp: ENSP00000407690.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.14G>T
  hgvsp: ENSP00000410371.1:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.427G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.14G>T
  hgvsp: ENSP00000415743.2:p.Arg5Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9786G>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg5Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

7-80276073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276073
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276073
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.17A>G
  hgvsp: ENSP00000378268.3:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.17A>G
  hgvsp: ENSP00000411411.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.17A>G
  hgvsp: ENSP00000396258.2:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.17A>G
  hgvsp: ENSP00000398760.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.17A>G
  hgvsp: ENSP00000441956.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.17A>G
  hgvsp: ENSP00000416388.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.17A>G
  hgvsp: ENSP00000407690.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.17A>G
  hgvsp: ENSP00000410371.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.17A>G
  hgvsp: ENSP00000308165.7:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.17A>G
  hgvsp: ENSP00000392298.2:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.17A>G
  hgvsp: ENSP00000415743.2:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.17A>G
  hgvsp: ENSP00000439543.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.17A>G
  hgvsp: ENSP00000433659.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.17A>G
  hgvsp: ENSP00000409762.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.17A>G
  hgvsp: ENSP00000399421.1:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.17A>G
  hgvsp: ENSP00000401863.2:p.Asn6Ser
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9783A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.430A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.304A>G
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn6Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

7-80276075-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276075
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276075
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.19T>G
  hgvsp: ENSP00000378268.3:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.19T>G
  hgvsp: ENSP00000392298.2:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.19T>G
  hgvsp: ENSP00000439543.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.19T>G
  hgvsp: ENSP00000308165.7:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.19T>G
  hgvsp: ENSP00000411411.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9781T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.19T>G
  hgvsp: ENSP00000407690.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.19T>G
  hgvsp: ENSP00000415743.2:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.19T>G
  hgvsp: ENSP00000396258.2:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.19T>G
  hgvsp: ENSP00000409762.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.19T>G
  hgvsp: ENSP00000398760.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.432T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.306T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.19T>G
  hgvsp: ENSP00000401863.2:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.19T>G
  hgvsp: ENSP00000410371.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.19T>G
  hgvsp: ENSP00000441956.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.19T>G
  hgvsp: ENSP00000416388.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.19T>G
  hgvsp: ENSP00000399421.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.19T>G
  hgvsp: ENSP00000433659.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys7Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS

7-80276076-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276076
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276076
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.20G>T
  hgvsp: ENSP00000378268.3:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.20G>T
  hgvsp: ENSP00000441956.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.20G>T
  hgvsp: ENSP00000439543.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.20G>T
  hgvsp: ENSP00000399421.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.20G>T
  hgvsp: ENSP00000433659.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.20G>T
  hgvsp: ENSP00000411411.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.20G>T
  hgvsp: ENSP00000409762.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.20G>T
  hgvsp: ENSP00000392298.2:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.20G>T
  hgvsp: ENSP00000410371.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.20G>T
  hgvsp: ENSP00000398760.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.20G>T
  hgvsp: ENSP00000416388.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.20G>T
  hgvsp: ENSP00000401863.2:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9780G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.20G>T
  hgvsp: ENSP00000308165.7:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.20G>T
  hgvsp: ENSP00000407690.1:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.307G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.20G>T
  hgvsp: ENSP00000396258.2:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.20G>T
  hgvsp: ENSP00000415743.2:p.Cys7Phe
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.433G>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys7Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

7-80276079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276079
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276079
    reference: chr 7
allele count: 4
allele frequency: 3.295381522795802e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.23G>A
  hgvsp: ENSP00000409762.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.23G>A
  hgvsp: ENSP00000411411.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.23G>A
  hgvsp: ENSP00000410371.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.23G>A
  hgvsp: ENSP00000441956.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.23G>A
  hgvsp: ENSP00000401863.2:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.23G>A
  hgvsp: ENSP00000407690.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.23G>A
  hgvsp: ENSP00000439543.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.23G>A
  hgvsp: ENSP00000399421.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.23G>A
  hgvsp: ENSP00000308165.7:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.23G>A
  hgvsp: ENSP00000433659.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.23G>A
  hgvsp: ENSP00000415743.2:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.23G>A
  hgvsp: ENSP00000396258.2:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.23G>A
  hgvsp: ENSP00000398760.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.310G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.23G>A
  hgvsp: ENSP00000392298.2:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.23G>A
  hgvsp: ENSP00000416388.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.436G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9777G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.23G>A
  hgvsp: ENSP00000378268.3:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly8Glu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

7-80276083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276083
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276083
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.27C>T
  hgvsp: ENST00000436384.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.27C>T
  hgvsp: ENST00000538969.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.27C>T
  hgvsp: ENST00000413265.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.27C>T
  hgvsp: ENST00000394788.3:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.27C>T
  hgvsp: ENST00000435819.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.27C>T
  hgvsp: ENST00000544133.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.27C>T
  hgvsp: ENST00000433696.2:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.27C>T
  hgvsp: ENST00000482059.2:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.27C>T
  hgvsp: ENST00000309881.7:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.27C>T
  hgvsp: ENST00000432207.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9773C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.27C>T
  hgvsp: ENST00000438020.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.440C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.27C>T
  hgvsp: ENST00000426978.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.27C>T
  hgvsp: ENST00000419819.2:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.314C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.27C>T
  hgvsp: ENST00000428497.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.27C>T
  hgvsp: ENST00000441034.2:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.27C>T
  hgvsp: ENST00000447544.2:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu9Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-80276086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276086
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276086
    reference: chr 7
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.30C>T
  hgvsp: ENST00000438020.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9770C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.30C>T
  hgvsp: ENST00000432207.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.30C>T
  hgvsp: ENST00000441034.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.30C>T
  hgvsp: ENST00000482059.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.317C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.30C>T
  hgvsp: ENST00000413265.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.30C>T
  hgvsp: ENST00000309881.7:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.30C>T
  hgvsp: ENST00000544133.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.30C>T
  hgvsp: ENST00000419819.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.30C>T
  hgvsp: ENST00000426978.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.30C>T
  hgvsp: ENST00000436384.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.30C>T
  hgvsp: ENST00000538969.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.30C>T
  hgvsp: ENST00000394788.3:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.30C>T
  hgvsp: ENST00000433696.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.30C>T
  hgvsp: ENST00000447544.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.30C>T
  hgvsp: ENST00000428497.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.30C>T
  hgvsp: ENST00000435819.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.443C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile10Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

7-80276087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276087
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276087
    reference: chr 7
allele count: 7
allele frequency: 5.767297773823059e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.31G>A
  hgvsp: ENSP00000410371.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.31G>A
  hgvsp: ENSP00000392298.2:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.31G>A
  hgvsp: ENSP00000396258.2:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.31G>A
  hgvsp: ENSP00000416388.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.31G>A
  hgvsp: ENSP00000308165.7:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.31G>A
  hgvsp: ENSP00000399421.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.31G>A
  hgvsp: ENSP00000411411.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.31G>A
  hgvsp: ENSP00000407690.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.31G>A
  hgvsp: ENSP00000398760.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.31G>A
  hgvsp: ENSP00000439543.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.31G>A
  hgvsp: ENSP00000415743.2:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.31G>A
  hgvsp: ENSP00000441956.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.444G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.318G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9769G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.31G>A
  hgvsp: ENSP00000378268.3:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.31G>A
  hgvsp: ENSP00000401863.2:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.31G>A
  hgvsp: ENSP00000409762.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.31G>A
  hgvsp: ENSP00000433659.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala11Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-80276097-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276097
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276097
    reference: chr 7
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.41T>G
  hgvsp: ENSP00000415743.2:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.41T>G
  hgvsp: ENSP00000396258.2:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.41T>G
  hgvsp: ENSP00000398760.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.41T>G
  hgvsp: ENSP00000433659.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.328T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.41T>G
  hgvsp: ENSP00000411411.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.41T>G
  hgvsp: ENSP00000416388.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.454T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.41T>G
  hgvsp: ENSP00000441956.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.41T>G
  hgvsp: ENSP00000392298.2:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.41T>G
  hgvsp: ENSP00000409762.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.41T>G
  hgvsp: ENSP00000308165.7:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.41T>G
  hgvsp: ENSP00000399421.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.41T>G
  hgvsp: ENSP00000378268.3:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.41T>G
  hgvsp: ENSP00000410371.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.41T>G
  hgvsp: ENSP00000439543.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9759T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.41T>G
  hgvsp: ENSP00000401863.2:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.41T>G
  hgvsp: ENSP00000407690.1:p.Val14Gly
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val14Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-80276099-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276099
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276099
    reference: chr 7
allele count: 12
allele frequency: 9.886144568387404e-5
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.43A>C
  hgvsp: ENSP00000410371.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.43A>C
  hgvsp: ENSP00000407690.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.43A>C
  hgvsp: ENSP00000308165.7:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.43A>C
  hgvsp: ENSP00000409762.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.43A>C
  hgvsp: ENSP00000416388.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.43A>C
  hgvsp: ENSP00000392298.2:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.43A>C
  hgvsp: ENSP00000378268.3:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.43A>C
  hgvsp: ENSP00000433659.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.43A>C
  hgvsp: ENSP00000399421.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.43A>C
  hgvsp: ENSP00000415743.2:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.330A>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9757A>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.43A>C
  hgvsp: ENSP00000411411.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.43A>C
  hgvsp: ENSP00000396258.2:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.43A>C
  hgvsp: ENSP00000398760.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.43A>C
  hgvsp: ENSP00000439543.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.43A>C
  hgvsp: ENSP00000441956.1:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.43A>C
  hgvsp: ENSP00000401863.2:p.Ile15Leu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.456A>C
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile15Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

7-80276100-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276100
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276100
    reference: chr 7
allele count: 7
allele frequency: 5.766917664892653e-5
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.44T>C
  hgvsp: ENSP00000416388.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.44T>C
  hgvsp: ENSP00000439543.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.44T>C
  hgvsp: ENSP00000392298.2:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.331T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.44T>C
  hgvsp: ENSP00000415743.2:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.44T>C
  hgvsp: ENSP00000396258.2:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.44T>C
  hgvsp: ENSP00000399421.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.44T>C
  hgvsp: ENSP00000411411.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.44T>C
  hgvsp: ENSP00000433659.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.44T>C
  hgvsp: ENSP00000398760.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.457T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.44T>C
  hgvsp: ENSP00000308165.7:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.44T>C
  hgvsp: ENSP00000401863.2:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.44T>C
  hgvsp: ENSP00000410371.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9756T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.44T>C
  hgvsp: ENSP00000407690.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.44T>C
  hgvsp: ENSP00000441956.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.44T>C
  hgvsp: ENSP00000378268.3:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.44T>C
  hgvsp: ENSP00000409762.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile15Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

7-80276101-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276101
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276101
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.45T>G
  hgvsp: ENSP00000407690.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.45T>G
  hgvsp: ENSP00000409762.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.45T>G
  hgvsp: ENSP00000308165.7:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.45T>G
  hgvsp: ENSP00000433659.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.332T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.45T>G
  hgvsp: ENSP00000441956.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.45T>G
  hgvsp: ENSP00000398760.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.458T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.45T>G
  hgvsp: ENSP00000378268.3:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.45T>G
  hgvsp: ENSP00000410371.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.45T>G
  hgvsp: ENSP00000439543.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.45T>G
  hgvsp: ENSP00000416388.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.45T>G
  hgvsp: ENSP00000415743.2:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.45T>G
  hgvsp: ENSP00000399421.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.45T>G
  hgvsp: ENSP00000396258.2:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9755T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.45T>G
  hgvsp: ENSP00000411411.1:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.45T>G
  hgvsp: ENSP00000401863.2:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.45T>G
  hgvsp: ENSP00000392298.2:p.Ile15Met
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile15Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

7-80276105-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276105
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276105
    reference: chr 7
allele count: 7
allele frequency: 5.76672762921589e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.49G>A
  hgvsp: ENSP00000378268.3:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.336G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.49G>A
  hgvsp: ENSP00000433659.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.49G>A
  hgvsp: ENSP00000396258.2:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.49G>A
  hgvsp: ENSP00000308165.7:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.49G>A
  hgvsp: ENSP00000415743.2:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.49G>A
  hgvsp: ENSP00000409762.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.49G>A
  hgvsp: ENSP00000399421.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.49G>A
  hgvsp: ENSP00000398760.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.49G>A
  hgvsp: ENSP00000410371.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9751G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.49G>A
  hgvsp: ENSP00000411411.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.49G>A
  hgvsp: ENSP00000441956.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.49G>A
  hgvsp: ENSP00000439543.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.462G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.49G>A
  hgvsp: ENSP00000392298.2:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.49G>A
  hgvsp: ENSP00000401863.2:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.49G>A
  hgvsp: ENSP00000416388.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.49G>A
  hgvsp: ENSP00000407690.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala17Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

7-80276108-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276108
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276108
    reference: chr 7
allele count: 9
allele frequency: 7.41534151767323e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.52G>A
  hgvsp: ENSP00000441956.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.52G>A
  hgvsp: ENSP00000416388.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.52G>A
  hgvsp: ENSP00000409762.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.52G>A
  hgvsp: ENSP00000433659.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.52G>A
  hgvsp: ENSP00000396258.2:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.52G>A
  hgvsp: ENSP00000415743.2:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.52G>A
  hgvsp: ENSP00000399421.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.465G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.52G>A
  hgvsp: ENSP00000410371.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.52G>A
  hgvsp: ENSP00000398760.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.52G>A
  hgvsp: ENSP00000308165.7:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.52G>A
  hgvsp: ENSP00000401863.2:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.52G>A
  hgvsp: ENSP00000411411.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.52G>A
  hgvsp: ENSP00000378268.3:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.52G>A
  hgvsp: ENSP00000439543.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.52G>A
  hgvsp: ENSP00000392298.2:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9748G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.52G>A
  hgvsp: ENSP00000407690.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.339G>A
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val18Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

7-80276111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276111
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276111
    reference: chr 7
allele count: 7
allele frequency: 5.767582888405511e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.55C>T
  hgvsp: ENST00000435819.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.342C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.55C>T
  hgvsp: ENST00000419819.2:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.55C>T
  hgvsp: ENST00000432207.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.55C>T
  hgvsp: ENST00000441034.2:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.55C>T
  hgvsp: ENST00000413265.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.55C>T
  hgvsp: ENST00000426978.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.468C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.55C>T
  hgvsp: ENST00000436384.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.55C>T
  hgvsp: ENST00000309881.7:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.55C>T
  hgvsp: ENST00000538969.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.55C>T
  hgvsp: ENST00000482059.2:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.55C>T
  hgvsp: ENST00000447544.2:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.55C>T
  hgvsp: ENST00000544133.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9745C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.55C>T
  hgvsp: ENST00000428497.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.55C>T
  hgvsp: ENST00000433696.2:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.55C>T
  hgvsp: ENST00000438020.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.55C>T
  hgvsp: ENST00000394788.3:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu19Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-80276115-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276115
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276115
    reference: chr 7
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.59C>A
  hgvsp: ENSP00000399421.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.59C>A
  hgvsp: ENSP00000401863.2:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.346C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.59C>A
  hgvsp: ENSP00000411411.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.59C>A
  hgvsp: ENSP00000433659.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.59C>A
  hgvsp: ENSP00000308165.7:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.59C>A
  hgvsp: ENSP00000441956.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.59C>A
  hgvsp: ENSP00000409762.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.59C>A
  hgvsp: ENSP00000392298.2:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9741C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.59C>A
  hgvsp: ENSP00000416388.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.59C>A
  hgvsp: ENSP00000398760.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.59C>A
  hgvsp: ENSP00000439543.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.59C>A
  hgvsp: ENSP00000410371.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.472C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.59C>A
  hgvsp: ENSP00000378268.3:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.59C>A
  hgvsp: ENSP00000396258.2:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.59C>A
  hgvsp: ENSP00000415743.2:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.59C>A
  hgvsp: ENSP00000407690.1:p.Ala20Asp
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala20Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-80276117-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276117
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276117
    reference: chr 7
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.61G>A
  hgvsp: ENSP00000439543.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.61G>A
  hgvsp: ENSP00000410371.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.61G>A
  hgvsp: ENSP00000416388.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.61G>A
  hgvsp: ENSP00000409762.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.61G>A
  hgvsp: ENSP00000441956.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.61G>A
  hgvsp: ENSP00000398760.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.61G>A
  hgvsp: ENSP00000378268.3:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.61G>A
  hgvsp: ENSP00000392298.2:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.61G>A
  hgvsp: ENSP00000411411.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.61G>A
  hgvsp: ENSP00000396258.2:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.348G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.61G>A
  hgvsp: ENSP00000399421.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.61G>A
  hgvsp: ENSP00000407690.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.61G>A
  hgvsp: ENSP00000415743.2:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.61G>A
  hgvsp: ENSP00000308165.7:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.61G>A
  hgvsp: ENSP00000401863.2:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.474G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.61G>A
  hgvsp: ENSP00000433659.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9739G>A
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val21Met
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

7-80276124-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276124
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276124
    reference: chr 7
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.68G>T
  hgvsp: ENSP00000410371.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.68G>T
  hgvsp: ENSP00000439543.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.68G>T
  hgvsp: ENSP00000308165.7:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.68G>T
  hgvsp: ENSP00000407690.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.68G>T
  hgvsp: ENSP00000409762.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.355G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.68G>T
  hgvsp: ENSP00000398760.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.68G>T
  hgvsp: ENSP00000416388.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.68G>T
  hgvsp: ENSP00000392298.2:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9732G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.68G>T
  hgvsp: ENSP00000399421.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.68G>T
  hgvsp: ENSP00000396258.2:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.68G>T
  hgvsp: ENSP00000441956.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.68G>T
  hgvsp: ENSP00000401863.2:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.68G>T
  hgvsp: ENSP00000415743.2:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.68G>T
  hgvsp: ENSP00000378268.3:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.68G>T
  hgvsp: ENSP00000433659.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.481G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.68G>T
  hgvsp: ENSP00000411411.1:p.Gly23Val
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly23Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-80276124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276124
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276124
    reference: chr 7
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.68G>A
  hgvsp: ENSP00000415743.2:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.68G>A
  hgvsp: ENSP00000410371.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.68G>A
  hgvsp: ENSP00000407690.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.68G>A
  hgvsp: ENSP00000392298.2:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.68G>A
  hgvsp: ENSP00000409762.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.68G>A
  hgvsp: ENSP00000416388.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.68G>A
  hgvsp: ENSP00000399421.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.68G>A
  hgvsp: ENSP00000401863.2:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.68G>A
  hgvsp: ENSP00000398760.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.68G>A
  hgvsp: ENSP00000308165.7:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.68G>A
  hgvsp: ENSP00000378268.3:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.68G>A
  hgvsp: ENSP00000441956.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.68G>A
  hgvsp: ENSP00000439543.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.68G>A
  hgvsp: ENSP00000433659.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.68G>A
  hgvsp: ENSP00000396258.2:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.68G>A
  hgvsp: ENSP00000411411.1:p.Gly23Glu
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9732G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.355G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.481G>A
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly23Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

7-80276145-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276145
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276145
    reference: chr 7
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.89G>T
  hgvsp: ENSP00000439543.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.502G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.89G>T
  hgvsp: ENSP00000308165.7:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.89G>T
  hgvsp: ENSP00000401863.2:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.89G>T
  hgvsp: ENSP00000392298.2:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.89G>T
  hgvsp: ENSP00000415743.2:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.89G>T
  hgvsp: ENSP00000410371.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.89G>T
  hgvsp: ENSP00000411411.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.89G>T
  hgvsp: ENSP00000433659.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.89G>T
  hgvsp: ENSP00000378268.3:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.89G>T
  hgvsp: ENSP00000441956.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.89G>T
  hgvsp: ENSP00000398760.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.89G>T
  hgvsp: ENSP00000407690.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9711G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.89G>T
  hgvsp: ENSP00000399421.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.89G>T
  hgvsp: ENSP00000396258.2:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.89G>T
  hgvsp: ENSP00000409762.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.376G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.89G>T
  hgvsp: ENSP00000416388.1:p.Gly30Val
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly30Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

7-80276161-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276161
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276160
    reference: chr 7
allele count: 5
allele frequency: 4.119634176485128e-5
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.107delA
  hgvsp: ENSP00000433659.1:p.Lys36ArgfsTer?
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.107delA
  hgvsp: ENSP00000401863.2:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.107delA
  hgvsp: ENSP00000439543.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.107delA
  hgvsp: ENSP00000409762.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.107delA
  hgvsp: ENSP00000441956.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.107delA
  hgvsp: ENSP00000392298.2:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.107delA
  hgvsp: ENSP00000407690.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.107delA
  hgvsp: ENSP00000398760.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.107delA
  hgvsp: ENSP00000308165.7:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.107delA
  hgvsp: ENSP00000411411.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.107delA
  hgvsp: ENSP00000396258.2:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.394delA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.107delA
  hgvsp: ENSP00000410371.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.107delA
  hgvsp: ENSP00000399421.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.107delA
  hgvsp: ENSP00000415743.2:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.107delA
  hgvsp: ENSP00000378268.3:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9693delA
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.107delA
  hgvsp: ENSP00000416388.1:p.Lys36ArgfsTer41
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.520delA
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys36ArgfsTer41
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: GA
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

7-80276170-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276170
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276170
    reference: chr 7
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.114T>G
  hgvsp: ENSP00000308165.7:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.114T>G
  hgvsp: ENSP00000392298.2:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.114T>G
  hgvsp: ENSP00000407690.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.114T>G
  hgvsp: ENSP00000396258.2:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.114T>G
  hgvsp: ENSP00000439543.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.114T>G
  hgvsp: ENSP00000410371.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.114T>G
  hgvsp: ENSP00000401863.2:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9686T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.114T>G
  hgvsp: ENSP00000416388.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.114T>G
  hgvsp: ENSP00000378268.3:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.114T>G
  hgvsp: ENSP00000415743.2:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.114T>G
  hgvsp: ENSP00000398760.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.114T>G
  hgvsp: ENSP00000399421.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.114T>G
  hgvsp: ENSP00000411411.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.527T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.114T>G
  hgvsp: ENSP00000433659.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.114T>G
  hgvsp: ENSP00000409762.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.114T>G
  hgvsp: ENSP00000441956.1:p.Ile38Met
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.401T>G
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile38Met
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

7-80276177-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276177
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276177
    reference: chr 7
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9679G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+1G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.534G>A
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.120+1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

7-80276177-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276177
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276177
    reference: chr 7
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9679G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+1G>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.534G>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.120+1G>T
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

7-80276180-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276180
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276180
    reference: chr 7
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9676C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.537C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+4C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.120+4C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-80276183-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276183
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276183
    reference: chr 7
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9673G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+7G>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.540G>A
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.120+7G>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

7-80276197-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276197
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276197
    reference: chr 7
allele count: 4
allele frequency: 3.296685183048445e-5
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9659A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.554A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+21A>T
  variant of: http://identifiers.org/hgnc/1663
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4946
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

7-80276200-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276200
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276200
    reference: chr 7
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.557C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9656C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+24C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4946
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS

http://identifiers.org/exac.variant/7-80276204-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276204
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276204
    reference: chr 7
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9652C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.561C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+28C>A
  variant of: http://identifiers.org/hgnc/1663
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

7-80276221-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276221
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276221
    reference: chr 7
allele count: 2
allele frequency: 1.648886177387175e-5
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.578T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9635T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+45T>G
  variant of: http://identifiers.org/hgnc/1663
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

7-80276225-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80276225
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80276223
    reference: chr 7
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.407+53_407+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-9627_-108-9626delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000480599
  gene symbol: CD36
  hgvsc: ENST00000480599.2:n.586_587delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.120+53_120+54delCT
  variant of: http://identifiers.org/hgnc/1663
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7286
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: TTC
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-80285807-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285807
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285807
    reference: chr 7
allele count: 1
allele frequency: 8.927455496634349e-6
allele num: 112014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.408-101C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.121-49C>A
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-80285811-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285811
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285811
    reference: chr 7
allele count: 85
allele frequency: 7.560528703324853e-4
allele num: 112426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.408-97T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.121-45T>C
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

7-80285818-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285818
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285818
    reference: chr 7
allele count: 1
allele frequency: 8.855356605210492e-6
allele num: 112926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.408-90T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.121-38T>C
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

7-80285819-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285819
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285819
    reference: chr 7
allele count: 2
allele frequency: 1.770757707222921e-5
allele num: 112946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.408-89A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.121-37A>G
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9664
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

7-80285819-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285819
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285819
    reference: chr 7
allele count: 1
allele frequency: 8.853788536114603e-6
allele num: 112946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.408-89A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.121-37A>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

7-80285830-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285830
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285830
    reference: chr 7
allele count: 1
allele frequency: 8.694291328313829e-6
allele num: 115018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.408-78A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.121-26A>G
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

7-80285837-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285837
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285837
    reference: chr 7
allele count: 1
allele frequency: 8.568099252861745e-6
allele num: 116712
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.408-71C>T
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-80285837-CTTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285837
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285834
    reference: chr 7
allele count: 1
allele frequency: 8.568099252861745e-6
allele num: 116712
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000411411
  ensembl transcript: ENST00000432207
  gene symbol: CD36
  hgvsc: ENST00000432207.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000398760
  ensembl transcript: ENST00000436384
  gene symbol: CD36
  hgvsc: ENST00000436384.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000416388
  ensembl transcript: ENST00000426978
  gene symbol: CD36
  hgvsc: ENST00000426978.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000415743
  ensembl transcript: ENST00000447544
  gene symbol: CD36
  hgvsc: ENST00000447544.2:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000407690
  ensembl transcript: ENST00000413265
  gene symbol: CD36
  hgvsc: ENST00000413265.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000441956
  ensembl transcript: ENST00000544133
  gene symbol: CD36
  hgvsc: ENST00000544133.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000392298
  ensembl transcript: ENST00000419819
  gene symbol: CD36
  hgvsc: ENST00000419819.2:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl transcript: ENST00000441109
  gene symbol: CD36
  hgvsc: ENST00000441109.2:n.408-68_408-66delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000396258
  ensembl transcript: ENST00000441034
  gene symbol: CD36
  hgvsc: ENST00000441034.2:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000308165
  ensembl transcript: ENST00000309881
  gene symbol: CD36
  hgvsc: ENST00000309881.7:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000401863
  ensembl transcript: ENST00000433696
  gene symbol: CD36
  hgvsc: ENST00000433696.2:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000439543
  ensembl transcript: ENST00000538969
  gene symbol: CD36
  hgvsc: ENST00000538969.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000399421
  ensembl transcript: ENST00000435819
  gene symbol: CD36
  hgvsc: ENST00000435819.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000433659
  ensembl transcript: ENST00000482059
  gene symbol: CD36
  hgvsc: ENST00000482059.2:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000431296
  ensembl transcript: ENST00000534394
  gene symbol: CD36
  hgvsc: ENST00000534394.1:c.-108-16_-108-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000378268
  ensembl transcript: ENST00000394788
  gene symbol: CD36
  hgvsc: ENST00000394788.3:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000410371
  ensembl transcript: ENST00000438020
  gene symbol: CD36
  hgvsc: ENST00000438020.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135218
  ensembl protein: ENSP00000409762
  ensembl transcript: ENST00000428497
  gene symbol: CD36
  hgvsc: ENST00000428497.1:c.121-16_121-14delATT
  variant of: http://identifiers.org/hgnc/1663
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: CTTA
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

7-80285839-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80285839
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 80285839
allele count: 2
allele frequency: 1.707212974818609e-5
allele num: 117150
alternate allele: G
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: T

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.283038234539389e-4
allele num: 7794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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FS
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VQSLOD
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QD
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MQ
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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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num of homozygotes: 0

African
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European (Finnish)
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East Asian
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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BaseQRankSum
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Latino
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allele frequency: 0.0e0
allele num: 5720
num of homozygotes: 0

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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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 2.699055330634278e-3
allele num: 7410
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Other
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East Asian
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DP
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: -1.46e-1

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

European (Non-Finnish)
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East Asian
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Other
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Latino
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African
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num of homozygotes: 0

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

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

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

Other
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South Asian
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East Asian
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Latino
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allele num: 11570
num of homozygotes: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

African
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allele frequency: 3.844675124951942e-4
allele num: 10404
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MQRankSum
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SIO_000300: 4.34e-1

QD
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: 2.0e-4

MQ
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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South Asian
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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allele num: 66724
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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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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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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African
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QD
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InbreedingCoeff
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
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

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

GenotypeDepth
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 3.456022118541559e-4
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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MQ
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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FS
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ClippingRankSum
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SIO_000300: 2.58e-1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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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: 9

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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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
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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

African
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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: 904
num of homozygotes: 0

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

Latino
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allele count: 5
allele frequency: 4.320027648176948e-4
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.99538355466291e-5
allele num: 66718
num of homozygotes: 0

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

VQSLOD
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SIO_000300: 3.12e0

BaseQRankSum
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ClippingRankSum
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MQ
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DP
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QD
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 57

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

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
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

East Asian
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allele count: 49
allele frequency: 5.677867902665122e-3
allele num: 8630
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South Asian
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allele num: 16512
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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FS
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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MQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

Latino
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Finnish)
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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QD
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DP
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African
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East Asian
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BaseQRankSum
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FS
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DP
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VQSLOD
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MQ
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QD
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MQRankSum
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InbreedingCoeff
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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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European (Finnish)
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African
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East Asian
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South Asian
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MQRankSum
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InbreedingCoeff
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QD
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DP
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FS
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VQSLOD
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MQ
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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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East Asian
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Latino
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European (Finnish)
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African
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 9.0e-4

MQ
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SIO_000300: 5.982e1

QD
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

Latino
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 1.948149258204705e-4
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

Other
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 16512
num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 0

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

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

African
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allele frequency: 5.765904285988853e-4
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66730
num of homozygotes: 0

East Asian
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Latino
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Other
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ReadPosRankSum
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MQ
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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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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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Latino
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Other
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MQ
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SIO_000300: 5.98e1

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

European (Non-Finnish)
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allele frequency: 1.640204697546254e-5
allele num: 60968
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

MQRankSum
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SIO_000300: -1.77e-1

QD
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ClippingRankSum
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FS
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MQ
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DP
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: -1.237e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

GenotypeDepth
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variant carriers: 13

GenotypeDepth
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variant carriers: 6

GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 5

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

African
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allele count: 83
allele frequency: 8.57792476229847e-3
allele num: 9676
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

Other
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allele count: 1
allele frequency: 1.165501165501166e-3
allele num: 858
num of homozygotes: 0

Latino
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allele count: 1
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allele num: 10740
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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -9.0e-2

ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 5.83e0

InbreedingCoeff
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SIO_000300: 4.6e-3

DP
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SIO_000300: 1.43457e6

QD
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SIO_000300: 1.492e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1892
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

Latino
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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: 1
allele frequency: 6.348400203148806e-5
allele num: 15752
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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
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SIO_000300: 1.65e0

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

DP
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SIO_000300: 1.481415e6

ReadPosRankSum
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SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 1.789e0

QD
type: SiteQuality
SIO_000300: 1.421e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

BaseQRankSum
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SIO_000300: -4.2e-1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 2
allele frequency: 1.269518852354958e-4
allele num: 15754
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6350
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61530
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.76e-1

MQ
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10774
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.347594261774788e-5
allele num: 15754
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61530
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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MQ
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DP
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.227596366314756e-4
allele num: 8146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10996
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

DP
type: SiteQuality
SIO_000300: 1.58632e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

MQ
type: SiteQuality
SIO_000300: 5.53e1

VQSLOD
type: SiteQuality
SIO_000300: -1.105e0

FS
type: SiteQuality
SIO_000300: 1.616e0

GenotypeDepth
all individuals: 315
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2192
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 497
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1011
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2073
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32834
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9469
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1766
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2281
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4505
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2317
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31115
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6107
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3025
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7895
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.994003597841295e-5
allele num: 10006
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63930
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -1.335e0

FS
type: SiteQuality
SIO_000300: 2.316e0

DP
type: SiteQuality
SIO_000300: 1.629996e6

MQ
type: SiteQuality
SIO_000300: 5.901e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.492e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

GenotypeDepth
all individuals: 2281
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2192
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 497
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 462
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 315
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32834
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 181
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2073
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1306
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1766
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3025
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6107
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31115
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7895
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.212709192335678e-4
allele num: 8246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
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: 11120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63930
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16068
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.901e1

FS
type: SiteQuality
SIO_000300: 2.316e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.335e0

DP
type: SiteQuality
SIO_000300: 1.629996e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.492e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.71e-1