18-19997785-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997785
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997785
    reference: chr 18
allele count: 49
allele frequency: 4.067672793079976e-4
allele num: 120462
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-11T>C
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20571
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13371
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26027
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1615
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6588
  bin: 9.75e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 7854
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 462
  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 3391
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16402
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8614
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 47
  allele frequency: 7.094125460363461e-4
  allele num: 66252
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

18-19997797-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997797
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997797
    reference: chr 18
allele count: 1
allele frequency: 8.330417687142833e-6
allele num: 120042
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-23T>C
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3859
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22482
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7276
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6546
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 7.25e1
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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
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 120
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genotype quality: GenotypeQuality
  all individuals: 1218
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 888
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11500
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8598
  num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-19997803-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997803
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997803
    reference: chr 18
allele count: 3
allele frequency: 2.495466569066197e-5
allele num: 120218
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-29G>T
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 20950
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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
  all individuals: 21
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 988
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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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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
  all individuals: 6550
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  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 2
  allele frequency: 1.959631589261219e-4
  allele num: 10206
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 8.700191404210893e-5
  allele num: 11494
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66126
  num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

18-19997804-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997804
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997804
    reference: chr 18
allele count: 1
allele frequency: 8.345573507811457e-6
allele num: 119824
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-30C>T
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9478
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 8.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2347
  bin: 3.25e1
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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
  all individuals: 6540
  bin: 9.75e1
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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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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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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: 541
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  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10132
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11474
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 6.119951040391677e-5
  allele num: 16340
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

18-19997806-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997806
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997806
    reference: chr 18
allele count: 25
allele frequency: 2.077585347206063e-4
allele num: 120332
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-32T>C
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17342
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 268
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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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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 21086
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 9.25e1
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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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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 25
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 2
  allele frequency: 1.741250217656277e-4
  allele num: 11486
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 23
  allele frequency: 3.475265177842918e-4
  allele num: 66182
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10224
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

18-19997810-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997810
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997810
    reference: chr 18
allele count: 1
allele frequency: 8.310065150910783e-6
allele num: 120336
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-36T>C
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16789
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
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genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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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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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 892
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population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11496
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.510847887834653e-5
  allele num: 66188
  num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/18-19997813-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997813
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997813
    reference: chr 18
allele count: 2
allele frequency: 1.663782776520698e-5
allele num: 120208
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-39G>T
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12524
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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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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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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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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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11478
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6582
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 2
  allele frequency: 3.023705853894533e-5
  allele num: 66144
  num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS

18-19997817-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997817
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997817
    reference: chr 18
allele count: 1
allele frequency: 8.327642777435419e-6
allele num: 120082
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-43C>T
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 6577
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.51285930408472e-5
  allele num: 66100
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population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6588
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 892
  num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

18-19997818-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19997818
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 19997818
    reference: chr 18
allele count: 1
allele frequency: 8.330417687142833e-6
allele num: 120042
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000212710
  ensembl protein: ENSP00000375220
  ensembl transcript: ENST00000391403
  gene symbol: CTAGE1
  hgvsc: ENST00000391403.2:c.-44T>C
  variant of: http://identifiers.org/hgnc/24346
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 8183
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16941
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3109
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6578
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6912
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8604
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11456
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.513546238837597e-5
  allele num: 66070
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

18-20513374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20513374
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20513374
    reference: chr 18
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-98-3343C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-252C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-98-3343C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-98-3343C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-98-3343C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000265943
  ensembl transcript: ENST00000578831
  gene symbol: RP11-739L10.1
  hgvsc: ENST00000578831.1:n.177+177G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-98-3343C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000264817
  ensembl transcript: ENST00000579822
  gene symbol: MIR4741
  hgvsc: ENST00000579822.1:n.63C>T
  variant of: http://identifiers.org/hgnc/41661
canonical: true
consequence: mature miRNA
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 2.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

18-20513376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20513376
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20513376
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 2
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000264817
  ensembl transcript: ENST00000579822
  gene symbol: MIR4741
  hgvsc: ENST00000579822.1:n.65G>A
  variant of: http://identifiers.org/hgnc/41661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-98-3341G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000265943
  ensembl transcript: ENST00000578831
  gene symbol: RP11-739L10.1
  hgvsc: ENST00000578831.1:n.177+175C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-98-3341G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-98-3341G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-250G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-98-3341G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-98-3341G>A
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: mature miRNA
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

18-20513432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20513432
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20513432
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 2
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-98-3285C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-98-3285C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-98-3285C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-194C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000265943
  ensembl transcript: ENST00000578831
  gene symbol: RP11-739L10.1
  hgvsc: ENST00000578831.1:n.177+119G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-98-3285C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-98-3285C>T
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 7.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

18-20513446-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20513446
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20513446
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 2
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-180G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-98-3271G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000265943
  ensembl transcript: ENST00000578831
  gene symbol: RP11-739L10.1
  hgvsc: ENST00000578831.1:n.177+105C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-98-3271G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-98-3271G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-98-3271G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-98-3271G>A
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

18-20516768-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516768
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516768
    reference: chr 18
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.-47G>A
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1874
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

18-20516780-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516780
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516780
    reference: chr 18
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.-35T>C
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

18-20516787-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516787
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516787
    reference: chr 18
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-28A>G
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32965
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

18-20516790-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516790
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516790
    reference: chr 18
allele count: 99
allele frequency: 8.166834402996156e-4
allele num: 121222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-25A>G
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32981
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10553
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

18-20516799-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516799
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516799
    reference: chr 18
allele count: 16
allele frequency: 1.319870652676038e-4
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.-16G>A
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-20516814-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516814
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516814
    reference: chr 18
allele count: 3
allele frequency: 2.474267616785431e-5
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.-1G>A
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-20516825-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516825
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516825
    reference: chr 18
allele count: 6
allele frequency: 4.948535233570863e-5
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.11C>T
  hgvsp: ENSP00000382630.2:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.11C>T
  hgvsp: ENSP00000354024.5:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.11C>T
  hgvsp: ENSP00000382627.2:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.11C>T
  hgvsp: ENSP00000463738.1:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.11C>T
  hgvsp: ENSP00000463439.1:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.11C>T
  hgvsp: ENSP00000464628.1:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.11C>T
  hgvsp: ENSP00000464284.1:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.11C>T
  hgvsp: ENSP00000382628.2:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.11C>T
  hgvsp: ENSP00000323050.5:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.11C>T
  hgvsp: ENSP00000463908.1:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.11C>T
  hgvsp: ENSP00000462390.1:p.Ser4Leu
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33092
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser4Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

18-20516826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516826
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516826
    reference: chr 18
allele count: 21
allele frequency: 1.73190162798753e-4
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.12G>A
  hgvsp: ENST00000327155.5:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.12G>A
  hgvsp: ENST00000360790.5:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.12G>A
  hgvsp: ENST00000579124.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.12G>A
  hgvsp: ENST00000582354.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.12G>A
  hgvsp: ENST00000583594.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.12G>A
  hgvsp: ENST00000399722.2:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.12G>A
  hgvsp: ENST00000581819.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.12G>A
  hgvsp: ENST00000399725.2:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.12G>A
  hgvsp: ENST00000399721.2:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.12G>A
  hgvsp: ENST00000583700.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.12G>A
  hgvsp: ENST00000577588.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
hgvs: p.Ser4Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

18-20516828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516828
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516828
    reference: chr 18
allele count: 7
allele frequency: 5.773005426625101e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.14G>A
  hgvsp: ENSP00000462390.1:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.14G>A
  hgvsp: ENSP00000463439.1:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.14G>A
  hgvsp: ENSP00000382630.2:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.14G>A
  hgvsp: ENSP00000463908.1:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.14G>A
  hgvsp: ENSP00000323050.5:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464628
  ensembl transcript: ENST00000583700
  gene symbol: RBBP8
  hgvsc: ENST00000583700.1:c.14G>A
  hgvsp: ENSP00000464628.1:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.14G>A
  hgvsp: ENSP00000464284.1:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.14G>A
  hgvsp: ENSP00000354024.5:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.14G>A
  hgvsp: ENSP00000463738.1:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.14G>A
  hgvsp: ENSP00000382628.2:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.14G>A
  hgvsp: ENSP00000382627.2:p.Gly5Glu
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Gly5Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-20516859-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516859
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516859
    reference: chr 18
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.45T>A
  hgvsp: ENSP00000464284.1:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.45T>A
  hgvsp: ENSP00000463439.1:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.45T>A
  hgvsp: ENSP00000354024.5:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.45T>A
  hgvsp: ENSP00000462390.1:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.45T>A
  hgvsp: ENSP00000323050.5:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.45T>A
  hgvsp: ENSP00000382630.2:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.45T>A
  hgvsp: ENSP00000382627.2:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.45T>A
  hgvsp: ENSP00000463908.1:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.45T>A
  hgvsp: ENSP00000382628.2:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.45T>A
  hgvsp: ENSP00000463738.1:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp15Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

18-20516860-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516860
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516860
    reference: chr 18
allele count: 10
allele frequency: 8.248375070111189e-5
allele num: 121236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.46A>G
  hgvsp: ENSP00000323050.5:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.46A>G
  hgvsp: ENSP00000464284.1:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.46A>G
  hgvsp: ENSP00000382628.2:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.46A>G
  hgvsp: ENSP00000463738.1:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.46A>G
  hgvsp: ENSP00000382627.2:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.46A>G
  hgvsp: ENSP00000462390.1:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.46A>G
  hgvsp: ENSP00000354024.5:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.46A>G
  hgvsp: ENSP00000463439.1:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.46A>G
  hgvsp: ENSP00000382630.2:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.46A>G
  hgvsp: ENSP00000463908.1:p.Thr16Ala
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 33118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr16Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

18-20516862-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516862
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516862
    reference: chr 18
allele count: 4
allele frequency: 3.299350028044475e-5
allele num: 121236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.48A>G
  hgvsp: ENST00000583594.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.48A>G
  hgvsp: ENST00000399725.2:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.48A>G
  hgvsp: ENST00000581819.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.48A>G
  hgvsp: ENST00000327155.5:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.48A>G
  hgvsp: ENST00000579124.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.48A>G
  hgvsp: ENST00000360790.5:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.48A>G
  hgvsp: ENST00000577588.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.48A>G
  hgvsp: ENST00000399721.2:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.48A>G
  hgvsp: ENST00000582354.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.48A>G
  hgvsp: ENST00000399722.2:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr16Thr
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

18-20516865-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516865
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516865
    reference: chr 18
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.51T>C
  hgvsp: ENST00000581819.1:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.51T>C
  hgvsp: ENST00000399721.2:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.51T>C
  hgvsp: ENST00000399725.2:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.51T>C
  hgvsp: ENST00000399722.2:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.51T>C
  hgvsp: ENST00000583594.1:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.51T>C
  hgvsp: ENST00000577588.1:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.51T>C
  hgvsp: ENST00000327155.5:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.51T>C
  hgvsp: ENST00000360790.5:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.51T>C
  hgvsp: ENST00000582354.1:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.51T>C
  hgvsp: ENST00000579124.1:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33125
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8622
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser17Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

18-20516868-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516868
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516868
    reference: chr 18
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.54T>C
  hgvsp: ENST00000581819.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.54T>C
  hgvsp: ENST00000399722.2:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.54T>C
  hgvsp: ENST00000399725.2:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.54T>C
  hgvsp: ENST00000360790.5:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.54T>C
  hgvsp: ENST00000579124.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.54T>C
  hgvsp: ENST00000582354.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.54T>C
  hgvsp: ENST00000583594.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.54T>C
  hgvsp: ENST00000327155.5:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.54T>C
  hgvsp: ENST00000577588.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.54T>C
  hgvsp: ENST00000399721.2:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser18Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-20516869-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516869
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516869
    reference: chr 18
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.55G>A
  hgvsp: ENSP00000382630.2:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.55G>A
  hgvsp: ENSP00000382628.2:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.55G>A
  hgvsp: ENSP00000354024.5:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.55G>A
  hgvsp: ENSP00000462390.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.55G>A
  hgvsp: ENSP00000382627.2:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.55G>A
  hgvsp: ENSP00000463908.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.55G>A
  hgvsp: ENSP00000323050.5:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.55G>A
  hgvsp: ENSP00000463439.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.55G>A
  hgvsp: ENSP00000464284.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.55G>A
  hgvsp: ENSP00000463738.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp19Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/18-20516879-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516879
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516879
    reference: chr 18
allele count: 7
allele frequency: 5.77634011090573e-5
allele num: 121184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.65A>C
  hgvsp: ENSP00000382627.2:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.65A>C
  hgvsp: ENSP00000323050.5:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.65A>C
  hgvsp: ENSP00000462390.1:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.65A>C
  hgvsp: ENSP00000354024.5:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.65A>C
  hgvsp: ENSP00000463738.1:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.65A>C
  hgvsp: ENSP00000463908.1:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.65A>C
  hgvsp: ENSP00000382630.2:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.65A>C
  hgvsp: ENSP00000464284.1:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.65A>C
  hgvsp: ENSP00000463439.1:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.65A>C
  hgvsp: ENSP00000382628.2:p.Asp22Ala
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp22Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

18-20516880-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516880
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516880
    reference: chr 18
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.66C>T
  hgvsp: ENST00000360790.5:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.66C>T
  hgvsp: ENST00000399725.2:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.66C>T
  hgvsp: ENST00000583594.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.66C>T
  hgvsp: ENST00000577588.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.66C>T
  hgvsp: ENST00000579124.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.66C>T
  hgvsp: ENST00000327155.5:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.66C>T
  hgvsp: ENST00000399722.2:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.66C>T
  hgvsp: ENST00000581819.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.66C>T
  hgvsp: ENST00000399721.2:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.66C>T
  hgvsp: ENST00000582354.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp22Asp
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

18-20516888-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516888
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516888
    reference: chr 18
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.74C>T
  hgvsp: ENSP00000323050.5:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000464284
  ensembl transcript: ENST00000577588
  gene symbol: RBBP8
  hgvsc: ENST00000577588.1:c.74C>T
  hgvsp: ENSP00000464284.1:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.74C>T
  hgvsp: ENSP00000382628.2:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.74C>T
  hgvsp: ENSP00000462390.1:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.74C>T
  hgvsp: ENSP00000463908.1:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.74C>T
  hgvsp: ENSP00000463738.1:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.74C>T
  hgvsp: ENSP00000382630.2:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.74C>T
  hgvsp: ENSP00000354024.5:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.74C>T
  hgvsp: ENSP00000463439.1:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.74C>T
  hgvsp: ENSP00000382627.2:p.Thr25Ile
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr25Ile
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

18-20516907-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516907
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516907
    reference: chr 18
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.93T>C
  hgvsp: ENST00000327155.5:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.93T>C
  hgvsp: ENST00000581819.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.93T>C
  hgvsp: ENST00000579124.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.93T>C
  hgvsp: ENST00000360790.5:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.93T>C
  hgvsp: ENST00000399722.2:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.93T>C
  hgvsp: ENST00000399721.2:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.93T>C
  hgvsp: ENST00000583594.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.93T>C
  hgvsp: ENST00000582354.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.93T>C
  hgvsp: ENST00000399725.2:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His31His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

18-20516908-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516908
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516909
    reference: chr 18
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.95dupA
  hgvsp: ENSP00000463738.1:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.95dupA
  hgvsp: ENSP00000323050.5:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.95dupA
  hgvsp: ENSP00000382630.2:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.95dupA
  hgvsp: ENSP00000354024.5:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.95dupA
  hgvsp: ENSP00000462390.1:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.95dupA
  hgvsp: ENSP00000463908.1:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.95dupA
  hgvsp: ENSP00000382627.2:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.95dupA
  hgvsp: ENSP00000463439.1:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.95dupA
  hgvsp: ENSP00000382628.2:p.Asp32GlufsTer2
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1552
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp32GlufsTer2
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

18-20516913-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516913
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516913
    reference: chr 18
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.99A>G
  hgvsp: ENST00000399722.2:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.99A>G
  hgvsp: ENST00000327155.5:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.99A>G
  hgvsp: ENST00000399721.2:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.99A>G
  hgvsp: ENST00000582354.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.99A>G
  hgvsp: ENST00000399725.2:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.99A>G
  hgvsp: ENST00000360790.5:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.99A>G
  hgvsp: ENST00000583594.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.99A>G
  hgvsp: ENST00000581819.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.99A>G
  hgvsp: ENST00000579124.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1549
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg33Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

18-20516923-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516923
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516923
    reference: chr 18
allele count: 1
allele frequency: 8.302889405513118e-6
allele num: 120440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109G>C
  hgvsp: ENSP00000323050.5:p.Gly37Arg
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109G>C
  hgvsp: ENSP00000382627.2:p.Gly37Arg
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109G>C
  hgvsp: ENSP00000463439.1:p.Gly37Arg
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109G>C
  hgvsp: ENSP00000382630.2:p.Gly37Arg
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109G>C
  hgvsp: ENSP00000462390.1:p.Gly37Arg
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109G>C
  hgvsp: ENSP00000354024.5:p.Gly37Arg
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109G>C
  hgvsp: ENSP00000382628.2:p.Gly37Arg
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109G>C
  hgvsp: ENSP00000463738.1:p.Gly37Arg
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109G>C
  hgvsp: ENSP00000463908.1:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly37Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

18-20516925-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516925
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516925
    reference: chr 18
allele count: 1
allele frequency: 8.323483877411729e-6
allele num: 120142
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+2T>C
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8444
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 8.25e1
  variant carriers: 0
hgvs: c.109+2T>C
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

18-20516929-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516929
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516929
    reference: chr 18
allele count: 371
allele frequency: 3.102473616430566e-3
allele num: 119582
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+6A>G
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 32443
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10352
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 13200
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 3.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 2.25e1
  variant carriers: 0
hgvs: c.109+6A>G
num of homozygotes: 3
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

18-20516942-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516942
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516942
    reference: chr 18
allele count: 1
allele frequency: 8.642892949127932e-6
allele num: 115702
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+19T>C
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30732
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41930
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

18-20516944-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516944
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516944
    reference: chr 18
allele count: 1
allele frequency: 8.717787774174425e-6
allele num: 114708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+21C>T
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5952
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

18-20516948-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516948
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516948
    reference: chr 18
allele count: 1
allele frequency: 8.859279209043553e-6
allele num: 112876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+25C>G
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS

18-20516949-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516949
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516949
    reference: chr 18
allele count: 1
allele frequency: 8.904085194287139e-6
allele num: 112308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+26A>G
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

18-20516950-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516950
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516950
    reference: chr 18
allele count: 2
allele frequency: 1.801834267284095e-5
allele num: 110998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+27G>A
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9233
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/18-20516951-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516951
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516951
    reference: chr 18
allele count: 1
allele frequency: 9.016156953260242e-6
allele num: 110912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+28C>A
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

18-20516983-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516983
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516983
    reference: chr 18
allele count: 55
allele frequency: 6.656661502711077e-4
allele num: 82624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+60T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+60T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+60T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+60T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+60T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.110-40T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+60T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+60T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+60T>C
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17800
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11283
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30925
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 9.75e1
  variant carriers: 51
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

18-20516986-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516986
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516986
    reference: chr 18
allele count: 1
allele frequency: 1.264734152881064e-5
allele num: 79068
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+63C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+63C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+63C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+63C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+63C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+63C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+63C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+63C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.110-37C>G
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15580
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

18-20516992-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20516992
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20516992
    reference: chr 18
allele count: 1
allele frequency: 1.357367792377022e-5
allele num: 73672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+69A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+69A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.110-31A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+69A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+69A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+69A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+69A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+69A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+69A>G
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5366
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-20517009-TATTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517009
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517004
    reference: chr 18
allele count: 1
allele frequency: 2.003686783681975e-5
allele num: 49908
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+87_109+91delATTTC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.110-13_110-9delATTTC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+87_109+91delATTTC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+87_109+91delATTTC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+87_109+91delATTTC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+87_109+91delATTTC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+87_109+91delATTTC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+87_109+91delATTTC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+87_109+91delATTTC
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29897
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: TATTTC
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

18-20517017-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517017
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517017
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 39942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+94T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+94T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.110-6T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+94T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+94T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+94T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+94T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+94T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+94T>C
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18829
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19492
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25240
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 2.75e1
  variant carriers: 0
hgvs: c.110-6T>C
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

18-20517021-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517021
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517021
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 35504
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+98A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+98A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+98A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.110-2A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+98A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+98A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+98A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+98A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+98A>G
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: splice acceptor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18204
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23453
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
hgvs: c.110-2A>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

18-20517029-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517029
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517029
    reference: chr 18
allele count: 534
allele frequency: 2.348698099929627e-2
allele num: 22736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+106G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.116G>C
  hgvsp: ENSP00000463908.1:p.Arg39Thr
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+106G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+106G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+106G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+106G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+106G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+106G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+106G>C
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 1.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 1.25e1
  variant carriers: 266
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28276
  bin: 2.5e0
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 15788
  bin: 7.5e0
  variant carriers: 473
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 2.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 2.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2775
  bin: 6.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 3.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 15800
  bin: 2.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 9.75e1
  variant carriers: 583
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 16
hgvs: p.Arg39Thr
num of homozygotes: 4
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

18-20517034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517034
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517034
    reference: chr 18
allele count: 2
allele frequency: 9.999000099990002e-5
allele num: 20002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+111C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.121C>T
  hgvsp: ENSP00000463908.1:p.Arg41Trp
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+111C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+111C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+111C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+111C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+111C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+111C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+111C>T
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30033
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30222
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg41Trp
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

18-20517035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517035
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517035
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 18438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+112G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+112G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+112G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+112G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+112G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.122G>A
  hgvsp: ENSP00000463908.1:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+112G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+112G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+112G>A
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30739
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14355
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14575
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg41Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

18-20517041-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517041
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517041
    reference: chr 18
allele count: 1
allele frequency: 6.379992344009187e-5
allele num: 15674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+118A>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+118A>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+118A>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+118A>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+118A>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+118A>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+118A>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.128A>T
  hgvsp: ENSP00000463908.1:p.Tyr43Phe
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+118A>T
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32531
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr43Phe
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

18-20517043-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517043
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517043
    reference: chr 18
allele count: 2
allele frequency: 1.310100877767588e-4
allele num: 15266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+120A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.130A>G
  hgvsp: ENSP00000463908.1:p.Met44Val
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+120A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+120A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+120A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+120A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+120A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+120A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+120A>G
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32836
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12176
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Met44Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

18-20517073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517073
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517073
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 6656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+150A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+150A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+150A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.160A>G
  hgvsp: ENSP00000463908.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+150A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+150A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+150A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+150A>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+150A>G
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30831
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2468
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met54Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

18-20517075-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517075
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517075
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 5856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+152G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+152G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+152G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463908
  ensembl transcript: ENST00000583594
  gene symbol: RBBP8
  hgvsc: ENST00000583594.1:c.162G>C
  hgvsp: ENSP00000463908.1:p.Met54Ile
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+152G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+152G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+152G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+152G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+152G>C
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29906
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27952
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Met54Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

18-20517102-TTCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517102
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517099
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 2718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+183_109+185delTCA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+183_109+185delTCA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+183_109+185delTCA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+183_109+185delTCA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+183_109+185delTCA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+183_109+185delTCA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+183_109+185delTCA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+183_109+185delTCA
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25710
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: TTCA
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/18-20517109-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20517109
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20517109
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 2168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.109+186C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.109+186C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.109+186C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.109+186C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.109+186C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.109+186C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.109+186C>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.109+186C>A
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24417
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19926
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

18-20526357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526357
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526357
    reference: chr 18
allele count: 61
allele frequency: 5.507801213522104e-4
allele num: 110752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.56C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-50C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-50C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-50C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-50C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-50C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-50C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-50C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-50C>T
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11369
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4671
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2499
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 5.75e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

18-20526361-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526361
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526362
    reference: chr 18
allele count: 1
allele frequency: 9.010632546404758e-6
allele num: 110980
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-43dupA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-43dupA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.63dupA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-43dupA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-43dupA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-43dupA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-43dupA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-43dupA
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-43dupA
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2434
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/18-20526363-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526363
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526363
    reference: chr 18
allele count: 5
allele frequency: 4.503693028283192e-5
allele num: 111020
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-44A>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.62A>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-44A>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-44A>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-44A>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-44A>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-44A>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-44A>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-44A>C
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8525
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7658
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4495
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

18-20526365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526365
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526365
    reference: chr 18
allele count: 1
allele frequency: 9.009658353755226e-6
allele num: 110992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-42G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-42G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-42G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-42G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-42G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-42G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.64G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-42G>A
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-42G>A
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

18-20526369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526369
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526369
    reference: chr 18
allele count: 3
allele frequency: 2.694981943620978e-5
allele num: 111318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.68C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-38C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-38C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-38C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-38C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-38C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-38C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-38C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-38C>T
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18185
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9267
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4708
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4002
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

18-20526371-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526371
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526371
    reference: chr 18
allele count: 2
allele frequency: 1.794558897423013e-5
allele num: 111448
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-36G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-36G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-36G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-36G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-36G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.70G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-36G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-36G>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-36G>C
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9467
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4750
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

18-20526372-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526372
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526372
    reference: chr 18
allele count: 3
allele frequency: 2.68976276292431e-5
allele num: 111534
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.71T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-35T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-35T>C
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4865
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4784
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-20526385-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526385
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526384
    reference: chr 18
allele count: 1
allele frequency: 8.808554868488276e-6
allele num: 113526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-20delC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-20delC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-20delC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-20delC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-20delC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-20delC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-20delC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.86delC
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-20delC
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4052
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2866
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: AC
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

18-20526387-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526387
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526388
    reference: chr 18
allele count: 21
allele frequency: 1.844953612594883e-4
allele num: 113824
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-16dupT
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.90dupT
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-16dupT
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-16dupT
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-16dupT
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-16dupT
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-16dupT
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-16dupT
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-16dupT
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27407
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10919
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-20526387-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526387
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526387
    reference: chr 18
allele count: 1
allele frequency: 8.785493393308968e-6
allele num: 113824
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-20C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-20C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.86C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-20C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-20C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-20C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-20C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-20C>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-20C>G
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7692
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

18-20526388-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526388
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526388
    reference: chr 18
allele count: 3
allele frequency: 2.630194634402946e-5
allele num: 114060
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.87T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-19T>C
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-19T>C
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5354
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ

18-20526392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526392
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526392
    reference: chr 18
allele count: 23
allele frequency: 2.005021270660437e-4
allele num: 114712
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-15C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-15C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-15C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-15C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-15C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.91C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-15C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-15C>T
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-15C>T
  variant of: http://identifiers.org/hgnc/9891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11263
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28361
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2889
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5389
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

18-20526403-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20526403
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 20526403
    reference: chr 18
allele count: 2
allele frequency: 1.714942292191868e-5
allele num: 116622
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463738
  ensembl transcript: ENST00000582354
  gene symbol: RBBP8
  hgvsc: ENST00000582354.1:c.110-4T>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382630
  ensembl transcript: ENST00000399725
  gene symbol: RBBP8
  hgvsc: ENST00000399725.2:c.110-4T>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382628
  ensembl transcript: ENST00000399722
  gene symbol: RBBP8
  hgvsc: ENST00000399722.2:c.110-4T>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000382627
  ensembl transcript: ENST00000399721
  gene symbol: RBBP8
  hgvsc: ENST00000399721.2:c.110-4T>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000463439
  ensembl transcript: ENST00000581819
  gene symbol: RBBP8
  hgvsc: ENST00000581819.1:c.110-4T>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101773
  ensembl transcript: ENST00000580892
  gene symbol: RBBP8
  hgvsc: ENST00000580892.1:n.102T>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000354024
  ensembl transcript: ENST00000360790
  gene symbol: RBBP8
  hgvsc: ENST00000360790.5:c.110-4T>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000323050
  ensembl transcript: ENST00000327155
  gene symbol: RBBP8
  hgvsc: ENST00000327155.5:c.110-4T>G
  variant of: http://identifiers.org/hgnc/9891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101773
  ensembl protein: ENSP00000462390
  ensembl transcript: ENST00000579124
  gene symbol: RBBP8
  hgvsc: ENST00000579124.1:c.110-4T>G
  variant of: http://identifiers.org/hgnc/9891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.75e1
  variant carriers: 0
hgvs: c.110-4T>G
num of homozygotes: 0
reference allele: T

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.949697796841489e-4
allele num: 10258
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

DP
type: SiteQuality
SIO_000300: 1.836184e6

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 1.099e1

FS
type: SiteQuality
SIO_000300: 5.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513683700653911e-5
allele num: 66064
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.800609e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.384e1

VQSLOD
type: SiteQuality
SIO_000300: -7.977e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

MQRankSum
type: SiteQuality
SIO_000300: -1.196e0

FS
type: SiteQuality
SIO_000300: 8.766999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.58e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.4e1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 5.128e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

DP
type: SiteQuality
SIO_000300: 1.784614e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65946
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.673e0

QD
type: SiteQuality
SIO_000300: 7.47e0

DP
type: SiteQuality
SIO_000300: 1.784684e6

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 5.345e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.214e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.94e-1

FS
type: SiteQuality
SIO_000300: 2.255e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.31e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.277e0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

QD
type: SiteQuality
SIO_000300: 1.247e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

DP
type: SiteQuality
SIO_000300: 1.782393e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.774499e6

VQSLOD
type: SiteQuality
SIO_000300: -3.7e-1

FS
type: SiteQuality
SIO_000300: 2.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
SIO_000300: 7.86e-1

QD
type: SiteQuality
SIO_000300: 7.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.427e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

DP
type: SiteQuality
SIO_000300: 1.761817e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.316e1

FS
type: SiteQuality
SIO_000300: 6.563e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.756212e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.541e0

FS
type: SiteQuality
SIO_000300: 1.017e0

QD
type: SiteQuality
SIO_000300: 1.226e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

DP
type: SiteQuality
SIO_000300: 1.754279e6

QD
type: SiteQuality
SIO_000300: 1.644e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

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

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

GenotypeQuality
all individuals: 100
bin: 2.5e0
variant carriers: 0

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

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

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

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

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

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.448e0

QD
type: SiteQuality
SIO_000300: 1.426e1

VQSLOD
type: SiteQuality
SIO_000300: 5.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 1.137e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

DP
type: SiteQuality
SIO_000300: 1.707e3

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

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

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

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

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 763
bin: 7.5e0
variant carriers: 2

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

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

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

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

African
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.757e3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.577e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.88e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.522e1

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

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

GenotypeQuality
all individuals: 357
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 3

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

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

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

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.031e3

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.41e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

GenotypeQuality
all individuals: 568
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.499e3

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.08e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

QD
type: SiteQuality
SIO_000300: 1.316e1

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8574
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1579
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.278e0

DP
type: SiteQuality
SIO_000300: 1.69783e6

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.249e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e0

QD
type: SiteQuality
SIO_000300: 1.154e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11560
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.001020346917952e-5
allele num: 66644
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
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SIO_000300: 4.38e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
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Other
type: Population
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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MQRankSum
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FS
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QD
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ReadPosRankSum
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DP
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VQSLOD
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SIO_000300: 1.94e-1

ClippingRankSum
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SIO_000300: -8.42e-1

BaseQRankSum
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SIO_000300: 4.71e0

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

European (Non-Finnish)
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allele frequency: 2.850798223502581e-4
allele num: 66648
num of homozygotes: 0

South Asian
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allele frequency: 3.635482307319437e-4
allele num: 16504
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East Asian
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allele frequency: 8.229021789522485e-3
allele num: 8628
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Latino
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allele num: 11562
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Other
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African
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -2.5e-1

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.976e1

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

European (Non-Finnish)
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allele count: 15
allele frequency: 2.250495108923963e-4
allele num: 66652
num of homozygotes: 0

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
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num of homozygotes: 0

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

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

East Asian
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South Asian
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allele num: 16504
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FS
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SIO_000300: 0.0e0

MQRankSum
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VQSLOD
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MQ
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DP
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ClippingRankSum
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QD
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InbreedingCoeff
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SIO_000300: -3.0e-4

ReadPosRankSum
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SIO_000300: 6.1e-1

BaseQRankSum
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SIO_000300: -2.733e0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.500180007200288e-5
allele num: 66664
num of homozygotes: 0

South Asian
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allele num: 16500
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FS
type: SiteQuality
SIO_000300: 5.77e-1

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

Other
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allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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African
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South Asian
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allele frequency: 3.635482307319437e-4
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DP
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 21

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

Latino
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allele frequency: 6.052222030088189e-4
allele num: 11566
num of homozygotes: 0

South Asian
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African
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allele frequency: 1.254584057131828e-3
allele num: 10362
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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allele frequency: 1.049947502624869e-4
allele num: 66670
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Other
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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QD
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MQ
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

South Asian
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East Asian
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African
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Latino
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European (Non-Finnish)
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Other
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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Latino
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African
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European (Non-Finnish)
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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MQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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African
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Other
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 2.424242424242424e-4
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQRankSum
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FS
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VQSLOD
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MQ
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QD
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GenotypeQuality
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variant carriers: 0

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

Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.159017153453871e-4
allele num: 8628
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African
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

Latino
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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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6606
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

East Asian
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allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

VQSLOD
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FS
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BaseQRankSum
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DP
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MQRankSum
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MQ
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ClippingRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

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

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

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

African
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allele 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

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

South Asian
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allele num: 16478
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InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.971e0

ReadPosRankSum
type: SiteQuality
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DP
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MQ
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FS
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QD
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MQRankSum
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 11528
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 count: 1
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allele num: 66460
num of homozygotes: 0

African
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South Asian
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East Asian
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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QD
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SIO_000300: 1.291e1

MQRankSum
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.953e1

InbreedingCoeff
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SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.690089e6

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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Latino
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allele frequency: 8.688097306689835e-5
allele num: 11510
num of homozygotes: 0

East Asian
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8492
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
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Latino
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allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66032
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MQ
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 233
allele frequency: 1.426297747306562e-2
allele num: 16336
num of homozygotes: 2

Latino
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allele count: 20
allele frequency: 1.748863238894718e-3
allele num: 11436
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 9.796238244514106e-5
allele num: 10208
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European (Non-Finnish)
type: Population
allele count: 108
allele frequency: 1.643785577303583e-3
allele num: 65702
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Other
type: Population
allele count: 9
allele frequency: 1.002227171492205e-2
allele num: 898
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.284565108094519e-5
allele num: 15912
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
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

BaseQRankSum
type: SiteQuality
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FS
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MQ
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InbreedingCoeff
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

QD
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GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10998
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62694
num of homozygotes: 0

South Asian
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allele frequency: 6.331518298087882e-5
allele num: 15794
num of homozygotes: 0

QD
type: SiteQuality
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DP
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ReadPosRankSum
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SIO_000300: -1.35e-1

VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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MQRankSum
type: SiteQuality
SIO_000300: -4.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

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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variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 15602
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.622007396353727e-5
allele num: 61652
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
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QD
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BaseQRankSum
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SIO_000300: -1.626e0

InbreedingCoeff
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SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
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DP
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SIO_000300: 1.494359e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.36e-1

FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
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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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.436663233779608e-5
allele num: 15536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61350
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 2.036e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.44e-1

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

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

Latino
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allele count: 1
allele frequency: 9.511128019783147e-5
allele num: 10514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.649294102124291e-5
allele num: 60632
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.194e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.91e-1

InbreedingCoeff
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SIO_000300: -1.9e-3

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.455013e6

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7562
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.044495508669313e-4
allele num: 9574
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10518
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60570
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BaseQRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 18
allele frequency: 4.047854637042367e-4
allele num: 44468
num of homozygotes: 0

East Asian
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Other
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allele num: 678
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South Asian
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allele frequency: 2.603369065849924e-3
allele num: 13060
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African
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Latino
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allele frequency: 2.888503755054881e-4
allele num: 6924
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5016
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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East Asian
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.35882436193801e-5
allele num: 42394
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South Asian
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Other
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
type: Population
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.550630005611386e-5
allele num: 39206
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European (Finnish)
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African
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Other
type: Population
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.804e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.5141e5

VQSLOD
type: SiteQuality
SIO_000300: -5.663e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e-1

GenotypeQuality
all individuals: 82
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1582
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15344
bin: 7.5e0
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GenotypeQuality
all individuals: 1138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
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GenotypeQuality
all individuals: 7093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1207
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25928
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.954210631096954e-5
allele num: 10046
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4384
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.43e-2

QD
type: SiteQuality
SIO_000300: 1.005e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

MQ
type: SiteQuality
SIO_000300: 4.921e1

MQRankSum
type: SiteQuality
SIO_000300: -4.692e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.213e0

DP
type: SiteQuality
SIO_000300: 6.39618e5

GenotypeQuality
all individuals: 185
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20930
bin: 7.5e0
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GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5608
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2112
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2782
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8914
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.13e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.523e1

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 5.5493e5

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

GenotypeQuality
all individuals: 23122
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1378
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 5.15577e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.355e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.056e0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 54

GenotypeQuality
all individuals: 1864
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 18

GenotypeQuality
all individuals: 107
bin: 8.25e1
variant carriers: 56

GenotypeQuality
all individuals: 1202
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variant carriers: 20

GenotypeQuality
all individuals: 82
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variant carriers: 8

GenotypeQuality
all individuals: 199
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variant carriers: 38

GenotypeQuality
all individuals: 2236
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variant carriers: 16

GenotypeQuality
all individuals: 109
bin: 7.75e1
variant carriers: 36

GenotypeQuality
all individuals: 433
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variant carriers: 25

GenotypeQuality
all individuals: 67
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variant carriers: 51

GenotypeQuality
all individuals: 28447
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variant carriers: 14

GenotypeQuality
all individuals: 778
bin: 2.75e1
variant carriers: 20

GenotypeQuality
all individuals: 123
bin: 7.25e1
variant carriers: 27

European (Non-Finnish)
type: Population
allele count: 389
allele frequency: 3.503873176004323e-2
allele num: 11102
num of homozygotes: 2

Latino
type: Population
allele count: 9
allele frequency: 1.212938005390836e-2
allele num: 742
num of homozygotes: 0

South Asian
type: Population
allele count: 102
allele frequency: 1.5625e-2
allele num: 6528
num of homozygotes: 2

African
type: Population
allele count: 11
allele frequency: 5.293551491819056e-3
allele num: 2078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 19
allele frequency: 1.463790446841294e-2
allele num: 1298
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 1.652892561983471e-2
allele num: 242
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.45e0

DP
type: SiteQuality
SIO_000300: 3.94643e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.94e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 65
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 239
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GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 719
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GenotypeQuality
all individuals: 1543
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 1118
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variant carriers: 0

GenotypeQuality
all individuals: 15750
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GenotypeQuality
all individuals: 43
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variant carriers: 1

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5978
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.093802345058626e-4
allele num: 9552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1090
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.49e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.455e1

DP
type: SiteQuality
SIO_000300: 3.63441e5

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 1

GenotypeQuality
all individuals: 2107
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GenotypeQuality
all individuals: 227
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 30614
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GenotypeQuality
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GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 962
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5714
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

QD
type: SiteQuality
SIO_000300: 1.146e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: -1.501e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.77e-2

DP
type: SiteQuality
SIO_000300: 3.47151e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 469
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variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.928268414963363e-4
allele num: 5186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

DP
type: SiteQuality
SIO_000300: 3.06993e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.294e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.12e-2

MQ
type: SiteQuality
SIO_000300: 5.915e1

MQRankSum
type: SiteQuality
SIO_000300: -8.68e-1

GenotypeQuality
all individuals: 32556
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.25e1
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GenotypeQuality
all individuals: 599
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GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1268
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 64
bin: 4.25e1
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GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.506024096385542e-3
allele num: 664
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.972386587771203e-4
allele num: 5070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.140000000000001e-2

DP
type: SiteQuality
SIO_000300: 3.0065e5

FS
type: SiteQuality
SIO_000300: 3.106e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.197e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.302e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
all individuals: 642
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29350
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 6157
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 105
bin: 6.75e1
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GenotypeQuality
all individuals: 704
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GenotypeQuality
all individuals: 279
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.25e1
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GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2110
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.790000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

QD
type: SiteQuality
SIO_000300: 8.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.586e0

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

DP
type: SiteQuality
SIO_000300: 1.78979e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.81e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.484e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.02e-2

DP
type: SiteQuality
SIO_000300: 1.67218e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.754e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.09755e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.395e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.78e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.524e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.7107e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.321e0

QD
type: SiteQuality
SIO_000300: 1.131e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 7705
bin: 9.75e1
variant carriers: 62

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.164033758926639e-4
allele num: 9242
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.484230055658627e-3
allele num: 10780
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.146018268364853e-4
allele num: 15546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 5.85480093676815e-4
allele num: 59780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.567e0

FS
type: SiteQuality
SIO_000300: 7.96e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

VQSLOD
type: SiteQuality
SIO_000300: 3.18e0

DP
type: SiteQuality
SIO_000300: 1.655766e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.259259259259259e-5
allele num: 10800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59940
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15558
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

QD
type: SiteQuality
SIO_000300: 7.26e0

MQ
type: SiteQuality
SIO_000300: 6.074e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

DP
type: SiteQuality
SIO_000300: 1.665145e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.668223675430402e-5
allele num: 59944
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.63460140537921e-4
allele num: 8254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.578781180928323e-4
allele num: 6334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.545e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 9.199999999999999e0

DP
type: SiteQuality
SIO_000300: 1.673188e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.668836153666433e-5
allele num: 59922
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15582
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.16e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.682691e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.409434687860531e-5
allele num: 15602
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.416042522348393e-4
allele num: 8278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10824
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.706705e6

VQSLOD
type: SiteQuality
SIO_000300: 9.72e-1

FS
type: SiteQuality
SIO_000300: 4.456e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2110
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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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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60232
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10826
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.280573697016263e-4
allele num: 15618
num of homozygotes: 1

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

VQSLOD
type: SiteQuality
SIO_000300: -3.119e-1

QD
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DP
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InbreedingCoeff
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SIO_000300: 6.4e-3

FS
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10832
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.97694017717907e-5
allele num: 60278
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.725166e6

FS
type: SiteQuality
SIO_000300: 1.2601e1

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

MQ
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -2.11e-1

VQSLOD
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.620955715489853e-5
allele num: 61692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8428
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e0

VQSLOD
type: SiteQuality
SIO_000300: -8.166e-1

DP
type: SiteQuality
SIO_000300: 1.804056e6

MQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

QD
type: SiteQuality
SIO_000300: 2.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 6.085e1

FS
type: SiteQuality
SIO_000300: 2.153e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 20

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10992
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

European (Non-Finnish)
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allele count: 19
allele frequency: 3.068475452196382e-4
allele num: 61920
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.334726973267453e-5
allele num: 15786
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.061345786457228e-4
allele num: 9422
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.814908e6

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

QD
type: SiteQuality
SIO_000300: 1.105e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.996e1

FS
type: SiteQuality
SIO_000300: 5.438e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10992
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61920
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9422
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15786
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.559575795383656e-4
allele num: 6412
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQ
type: SiteQuality
SIO_000300: 5.996e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.814908e6

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.105e1

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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62060
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6420
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East Asian
type: Population
allele count: 3
allele frequency: 3.544423440453686e-4
allele num: 8464
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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Latino
type: Population
allele count: 0
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allele num: 11012
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African
type: Population
allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.81925e6

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 20

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.311537490532694e-5
allele num: 15844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 1
allele frequency: 1.052631578947368e-4
allele num: 9500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 21
allele frequency: 3.35989248344053e-4
allele num: 62502
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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QD
type: SiteQuality
SIO_000300: 1.266e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.933e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.832099e6

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.55e-1