http://identifiers.org/exac.variant/8-146005574-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146005574
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146005574
    reference: chr 8
allele count: 1
allele frequency: 4.843084075939558e-5
allele num: 20648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000437056
  ensembl transcript: ENST00000534445
  gene symbol: ZNF34
  hgvsc: ENST00000534445.1:c.9+43G>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl transcript: ENST00000527740
  gene symbol: ZNF34
  hgvsc: ENST00000527740.1:n.82+39G>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000341528
  ensembl transcript: ENST00000343459
  gene symbol: ZNF34
  hgvsc: ENST00000343459.4:c.9+43G>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000396894
  ensembl transcript: ENST00000429371
  gene symbol: ZNF34
  hgvsc: ENST00000429371.2:c.-55+39G>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000434049
  ensembl transcript: ENST00000534337
  gene symbol: ZNF34
  hgvsc: ENST00000534337.1:c.-55+39G>T
  variant of: http://identifiers.org/hgnc/13098
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

8-146005577-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146005577
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146005577
    reference: chr 8
allele count: 6
allele frequency: 2.903038513644281e-4
allele num: 20668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000437056
  ensembl transcript: ENST00000534445
  gene symbol: ZNF34
  hgvsc: ENST00000534445.1:c.9+40C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000341528
  ensembl transcript: ENST00000343459
  gene symbol: ZNF34
  hgvsc: ENST00000343459.4:c.9+40C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl transcript: ENST00000527740
  gene symbol: ZNF34
  hgvsc: ENST00000527740.1:n.82+36C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000396894
  ensembl transcript: ENST00000429371
  gene symbol: ZNF34
  hgvsc: ENST00000429371.2:c.-55+36C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000434049
  ensembl transcript: ENST00000534337
  gene symbol: ZNF34
  hgvsc: ENST00000534337.1:c.-55+36C>T
  variant of: http://identifiers.org/hgnc/13098
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5026
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-146005624-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146005624
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146005624
    reference: chr 8
allele count: 1
allele frequency: 4.774637127578304e-5
allele num: 20944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196378
  ensembl transcript: ENST00000527740
  gene symbol: ZNF34
  hgvsc: ENST00000527740.1:n.71T>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000437056
  ensembl transcript: ENST00000534445
  gene symbol: ZNF34
  hgvsc: ENST00000534445.1:c.2T>C
  hgvsp: ENSP00000437056.1:p.Met1?
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000434049
  ensembl transcript: ENST00000534337
  gene symbol: ZNF34
  hgvsc: ENST00000534337.1:c.-66T>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000341528
  ensembl transcript: ENST00000343459
  gene symbol: ZNF34
  hgvsc: ENST00000343459.4:c.2T>C
  hgvsp: ENSP00000341528.4:p.Met1?
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000396894
  ensembl transcript: ENST00000429371
  gene symbol: ZNF34
  hgvsc: ENST00000429371.2:c.-66T>C
  variant of: http://identifiers.org/hgnc/13098
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5033
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

8-146005635-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146005635
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146005635
    reference: chr 8
allele count: 28
allele frequency: 1.330419082010833e-3
allele num: 21046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196378
  ensembl transcript: ENST00000527740
  gene symbol: ZNF34
  hgvsc: ENST00000527740.1:n.60C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000434049
  ensembl transcript: ENST00000534337
  gene symbol: ZNF34
  hgvsc: ENST00000534337.1:c.-77C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000396894
  ensembl transcript: ENST00000429371
  gene symbol: ZNF34
  hgvsc: ENST00000429371.2:c.-77C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000437056
  ensembl transcript: ENST00000534445
  gene symbol: ZNF34
  hgvsc: ENST00000534445.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000341528
  ensembl transcript: ENST00000343459
  gene symbol: ZNF34
  hgvsc: ENST00000343459.4:c.-10C>T
  variant of: http://identifiers.org/hgnc/13098
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5045
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

8-146005647-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146005647
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146005647
    reference: chr 8
allele count: 7
allele frequency: 3.299396681749623e-4
allele num: 21216
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000341528
  ensembl transcript: ENST00000343459
  gene symbol: ZNF34
  hgvsc: ENST00000343459.4:c.-22A>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000437056
  ensembl transcript: ENST00000534445
  gene symbol: ZNF34
  hgvsc: ENST00000534445.1:c.-22A>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196378
  ensembl transcript: ENST00000527740
  gene symbol: ZNF34
  hgvsc: ENST00000527740.1:n.48A>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000434049
  ensembl transcript: ENST00000534337
  gene symbol: ZNF34
  hgvsc: ENST00000534337.1:c.-89A>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000396894
  ensembl transcript: ENST00000429371
  gene symbol: ZNF34
  hgvsc: ENST00000429371.2:c.-89A>C
  variant of: http://identifiers.org/hgnc/13098
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

8-146005648-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146005648
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146005648
    reference: chr 8
allele count: 3
allele frequency: 1.413760603204524e-4
allele num: 21220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000396894
  ensembl transcript: ENST00000429371
  gene symbol: ZNF34
  hgvsc: ENST00000429371.2:c.-90C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196378
  ensembl transcript: ENST00000527740
  gene symbol: ZNF34
  hgvsc: ENST00000527740.1:n.47C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000437056
  ensembl transcript: ENST00000534445
  gene symbol: ZNF34
  hgvsc: ENST00000534445.1:c.-23C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000341528
  ensembl transcript: ENST00000343459
  gene symbol: ZNF34
  hgvsc: ENST00000343459.4:c.-23C>T
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000434049
  ensembl transcript: ENST00000534337
  gene symbol: ZNF34
  hgvsc: ENST00000534337.1:c.-90C>T
  variant of: http://identifiers.org/hgnc/13098
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5038
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

8-146005655-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146005655
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146005655
    reference: chr 8
allele count: 1
allele frequency: 4.691311690748734e-5
allele num: 21316
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000341528
  ensembl transcript: ENST00000343459
  gene symbol: ZNF34
  hgvsc: ENST00000343459.4:c.-30T>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000434049
  ensembl transcript: ENST00000534337
  gene symbol: ZNF34
  hgvsc: ENST00000534337.1:c.-97T>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196378
  ensembl transcript: ENST00000527740
  gene symbol: ZNF34
  hgvsc: ENST00000527740.1:n.40T>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000437056
  ensembl transcript: ENST00000534445
  gene symbol: ZNF34
  hgvsc: ENST00000534445.1:c.-30T>C
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000396894
  ensembl transcript: ENST00000429371
  gene symbol: ZNF34
  hgvsc: ENST00000429371.2:c.-97T>C
  variant of: http://identifiers.org/hgnc/13098
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5036
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

8-146005666-CTAAAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146005666
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146005661
    reference: chr 8
allele count: 83
allele frequency: 3.873798189116027e-3
allele num: 21426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000437056
  ensembl transcript: ENST00000534445
  gene symbol: ZNF34
  hgvsc: ENST00000534445.1:c.-40-6_-40-2delTTTTA
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000341528
  ensembl transcript: ENST00000343459
  gene symbol: ZNF34
  hgvsc: ENST00000343459.4:c.-40-6_-40-2delTTTTA
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl transcript: ENST00000527740
  gene symbol: ZNF34
  hgvsc: ENST00000527740.1:n.30-6_30-2delTTTTA
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000434049
  ensembl transcript: ENST00000534337
  gene symbol: ZNF34
  variant of: http://identifiers.org/hgnc/13098
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196378
  ensembl protein: ENSP00000396894
  ensembl transcript: ENST00000429371
  gene symbol: ZNF34
  hgvsc: ENST00000429371.2:c.-107-6_-107-2delTTTTA
  variant of: http://identifiers.org/hgnc/13098
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5101
  bin: 9.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: c.-40-6_-40-2delTTTTA
num of homozygotes: 4
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: CTAAAA
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

8-146015140-T-TGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015140
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015142
    reference: chr 8
allele count: 2
allele frequency: 1.649947201689546e-5
allele num: 121216
alternate allele: TGG
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11059
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6663
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genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3677
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 410
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13772
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 3966
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16496
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11576
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8644
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10380
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-146015143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015143
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015143
    reference: chr 8
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: A
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
  all individuals: 24
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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  bin: 6.75e1
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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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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
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: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 265
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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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  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 3954
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10382
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11576
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.500555205426008e-5
  allele num: 66642
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16498
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD

8-146015145-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015145
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015145
    reference: chr 8
allele count: 3
allele frequency: 2.473737157181259e-5
allele num: 121274
alternate allele: G
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11176
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
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genotype depth: GenotypeDepth
  all individuals: 83
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 62
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
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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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  variant carriers: 2
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3944
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
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: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1500
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 81
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  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8644
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11576
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6614
  num of homozygotes: 0
population: African
  type: Population
  allele count: 3
  allele frequency: 2.889060092449923e-4
  allele num: 10384
  num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

8-146015150-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015150
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015150
    reference: chr 8
allele count: 3
allele frequency: 2.473247704001715e-5
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.716G>C
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 83
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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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  variant carriers: 0
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: 3
  allele frequency: 2.591568762957844e-4
  allele num: 11576
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66660
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6614
  num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

8-146015152-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015152
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015152
    reference: chr 8
allele count: 8
allele frequency: 6.595218466611707e-5
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.556C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*366C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.714C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 62
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3925
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34642
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3696
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13831
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 9.75e1
  variant carriers: 8
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

8-146015154-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015154
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015154
    reference: chr 8
allele count: 897
allele frequency: 7.394522941981435e-3
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*35A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*364A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.712A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.716A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.540A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*35A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.554A>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11310
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 14939
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19399
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 9.75e1
  variant carriers: 634
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 9.75e1
  variant carriers: 849
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13810
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34618
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 45
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

8-146015156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015156
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015156
    reference: chr 8
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*33C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*362C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.710C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.*33C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.714C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.538C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.552C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35187
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-146015161-AAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015161
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015159
    reference: chr 8
allele count: 5
allele frequency: 4.1209244057627e-5
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*26_*27delGT
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.*26_*27delGT
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*355_*356delGT
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.531_532delGT
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.703_704delGT
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.707_708delGT
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*26_*27delGT
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.545_546delGT
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3947
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: AAC
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

8-146015165-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015165
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015165
    reference: chr 8
allele count: 3
allele frequency: 2.47239162683369e-5
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.705G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.701G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*24G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.529G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.*24G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.543G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*353G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-146015174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015174
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015174
    reference: chr 8
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*15A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.*15A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.534A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.692A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.520A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.696A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*344A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3743
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

8-146015178-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015178
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015178
    reference: chr 8
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.530C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.688C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.692C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.*11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*340C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.516C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff

8-146015179-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015179
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015178
    reference: chr 8
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*9delG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*338delG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.528delG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.*9delG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*9delG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.*9delG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.686delG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.690delG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.514delG
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35521
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3744
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: GC
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS

8-146015182-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015182
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015182
    reference: chr 8
allele count: 16
allele frequency: 1.318239491159556e-4
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.684G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*7G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.512G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.526G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.*7G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.688G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*336G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

8-146015186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015186
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015186
    reference: chr 8
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*332C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.*3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.*3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.684C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.*3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.*3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.508C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.522C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.680C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35556
  bin: 6.25e1
  variant carriers: 0
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: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-146015207-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015207
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015207
    reference: chr 8
allele count: 5
allele frequency: 4.119091163725636e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.756G>T
  hgvsp: ENST00000394920.2:c.756G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.756G>T
  hgvsp: ENST00000528957.1:c.756G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.429G>T
  hgvsp: ENST00000527914.1:c.429G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.756G>T
  hgvsp: ENST00000262584.3:c.756G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.663G>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.693G>T
  hgvsp: ENST00000533397.1:c.693G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.501G>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*311G>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*338G>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.659G>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.487G>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val252Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

8-146015210-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015210
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015210
    reference: chr 8
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.690T>C
  hgvsp: ENST00000533397.1:c.690T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*335T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.656T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.484T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*308T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.426T>C
  hgvsp: ENST00000527914.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.498T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.660T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.753T>C
  hgvsp: ENST00000528957.1:c.753T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.753T>C
  hgvsp: ENST00000394920.2:c.753T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.753T>C
  hgvsp: ENST00000262584.3:c.753T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr251Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

8-146015214-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015214
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015214
    reference: chr 8
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.749A>T
  hgvsp: ENSP00000262584.3:p.Lys250Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.656A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.749A>T
  hgvsp: ENSP00000433464.2:p.Lys250Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*331A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.686A>T
  hgvsp: ENSP00000435313.1:p.Lys229Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*304A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.422A>T
  hgvsp: ENSP00000436460.1:p.Lys141Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.749A>T
  hgvsp: ENSP00000378378.2:p.Lys250Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.480A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.494A>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.652A>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19658
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys250Met
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

8-146015223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015223
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015223
    reference: chr 8
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.471G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.643G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.740G>A
  hgvsp: ENSP00000433464.2:p.Arg247Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*295G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*322G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.413G>A
  hgvsp: ENSP00000436460.1:p.Arg138Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.740G>A
  hgvsp: ENSP00000378378.2:p.Arg247Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.740G>A
  hgvsp: ENSP00000262584.3:p.Arg247Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.677G>A
  hgvsp: ENSP00000435313.1:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.485G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.647G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg247Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

8-146015224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015224
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015224
    reference: chr 8
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.646C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.412C>T
  hgvsp: ENSP00000436460.1:p.Arg138Trp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.739C>T
  hgvsp: ENSP00000378378.2:p.Arg247Trp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*294C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.739C>T
  hgvsp: ENSP00000262584.3:p.Arg247Trp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.642C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.739C>T
  hgvsp: ENSP00000433464.2:p.Arg247Trp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.470C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.676C>T
  hgvsp: ENSP00000435313.1:p.Arg226Trp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*321C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.484C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg247Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

8-146015227-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015227
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015227
    reference: chr 8
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.736C>T
  hgvsp: ENSP00000433464.2:p.Leu246Phe
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*318C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.643C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.481C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.736C>T
  hgvsp: ENSP00000262584.3:p.Leu246Phe
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.467C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.639C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.736C>T
  hgvsp: ENSP00000378378.2:p.Leu246Phe
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.673C>T
  hgvsp: ENSP00000435313.1:p.Leu225Phe
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.409C>T
  hgvsp: ENSP00000436460.1:p.Leu137Phe
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*291C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu246Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-146015228-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015228
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015228
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.466T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.735T>G
  hgvsp: ENST00000262584.3:c.735T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.638T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.735T>G
  hgvsp: ENST00000394920.2:c.735T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.735T>G
  hgvsp: ENST00000528957.1:c.735T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.408T>G
  hgvsp: ENST00000527914.1:c.408T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.672T>G
  hgvsp: ENST00000533397.1:c.672T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*317T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*290T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.480T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.642T>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg245Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

8-146015229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015229
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015229
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.479G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.465G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.407G>A
  hgvsp: ENSP00000436460.1:p.Arg136His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.734G>A
  hgvsp: ENSP00000433464.2:p.Arg245His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.734G>A
  hgvsp: ENSP00000378378.2:p.Arg245His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.637G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*316G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.734G>A
  hgvsp: ENSP00000262584.3:p.Arg245His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.641G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.671G>A
  hgvsp: ENSP00000435313.1:p.Arg224His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*289G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg245His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

8-146015234-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015234
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015234
    reference: chr 8
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.474T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.666T>C
  hgvsp: ENST00000533397.1:c.666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*311T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.729T>C
  hgvsp: ENST00000394920.2:c.729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.460T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.402T>C
  hgvsp: ENST00000527914.1:c.402T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.729T>C
  hgvsp: ENST00000262584.3:c.729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.636T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*284T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.729T>C
  hgvsp: ENST00000528957.1:c.729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.632T>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr243Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-146015264-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015264
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015264
    reference: chr 8
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.606C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*281C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.636C>T
  hgvsp: ENST00000533397.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.699C>T
  hgvsp: ENST00000394920.2:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.372C>T
  hgvsp: ENST00000527914.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.444C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.430C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.699C>T
  hgvsp: ENST00000528957.1:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.602C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.699C>T
  hgvsp: ENST00000262584.3:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*254C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg233Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

8-146015286-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015286
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015286
    reference: chr 8
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.677G>A
  hgvsp: ENSP00000262584.3:p.Arg226His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.350G>A
  hgvsp: ENSP00000436460.1:p.Arg117His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.422G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.677G>A
  hgvsp: ENSP00000433464.2:p.Arg226His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*232G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*259G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.408G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.580G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.614G>A
  hgvsp: ENSP00000435313.1:p.Arg205His
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.584G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.677G>A
  hgvsp: ENSP00000378378.2:p.Arg226His
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg226His
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

8-146015287-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015287
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015287
    reference: chr 8
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.676C>T
  hgvsp: ENSP00000433464.2:p.Arg226Cys
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.583C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.676C>T
  hgvsp: ENSP00000262584.3:p.Arg226Cys
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.613C>T
  hgvsp: ENSP00000435313.1:p.Arg205Cys
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*231C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.579C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*258C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.421C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.349C>T
  hgvsp: ENSP00000436460.1:p.Arg117Cys
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.676C>T
  hgvsp: ENSP00000378378.2:p.Arg226Cys
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.407C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg226Cys
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

8-146015297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015297
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015297
    reference: chr 8
allele count: 5
allele frequency: 4.134896875671921e-5
allele num: 120922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.411C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*221C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.339C>T
  hgvsp: ENST00000527914.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.397C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.666C>T
  hgvsp: ENST00000262584.3:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.603C>T
  hgvsp: ENST00000533397.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.666C>T
  hgvsp: ENST00000528957.1:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.573C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*248C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.666C>T
  hgvsp: ENST00000394920.2:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.569C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro222Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

8-146015306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015306
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015306
    reference: chr 8
allele count: 1
allele frequency: 8.29132395860971e-6
allele num: 120608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.402C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.594C>T
  hgvsp: ENST00000533397.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*212C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.657C>T
  hgvsp: ENST00000262584.3:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.388C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.330C>T
  hgvsp: ENST00000527914.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*239C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.564C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.657C>T
  hgvsp: ENST00000528957.1:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.560C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.657C>T
  hgvsp: ENST00000394920.2:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11181
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile219Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

8-146015308-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015308
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015308
    reference: chr 8
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.655A>G
  hgvsp: ENSP00000433464.2:p.Ile219Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*210A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.655A>G
  hgvsp: ENSP00000378378.2:p.Ile219Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.562A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.328A>G
  hgvsp: ENSP00000436460.1:p.Ile110Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.655A>G
  hgvsp: ENSP00000262584.3:p.Ile219Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.558A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.592A>G
  hgvsp: ENSP00000435313.1:p.Ile198Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.400A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.386A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*237A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile219Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-146015312-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015312
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015312
    reference: chr 8
allele count: 1
allele frequency: 8.316423272678886e-6
allele num: 120244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.588G>A
  hgvsp: ENST00000533397.1:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.651G>A
  hgvsp: ENST00000262584.3:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.396G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*206G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.324G>A
  hgvsp: ENST00000527914.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.382G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.651G>A
  hgvsp: ENST00000528957.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.554G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*233G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.558G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.651G>A
  hgvsp: ENST00000394920.2:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln217Gln
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

8-146015321-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015321
    reference: chr 8
allele count: 1
allele frequency: 8.347106058329577e-6
allele num: 119802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.579C>T
  hgvsp: ENST00000533397.1:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.642C>T
  hgvsp: ENST00000262584.3:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*224C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.387C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.642C>T
  hgvsp: ENST00000528957.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.373C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.315C>T
  hgvsp: ENST00000527914.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.642C>T
  hgvsp: ENST00000394920.2:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.549C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.545C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*197C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly214Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

8-146015342-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015342
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015342
    reference: chr 8
allele count: 8
allele frequency: 6.790364472813078e-5
allele num: 117814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.294G>A
  hgvsp: ENST00000527914.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.621G>A
  hgvsp: ENST00000262584.3:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.558G>A
  hgvsp: ENST00000533397.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*176G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.352G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.528G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.366G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.621G>A
  hgvsp: ENST00000528957.1:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.621G>A
  hgvsp: ENST00000394920.2:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.524G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*203G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9378
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val207Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

8-146015350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015350
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015350
    reference: chr 8
allele count: 1
allele frequency: 8.555051758063135e-6
allele num: 116890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-3C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-3C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.616-3C>T
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

8-146015351-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015351
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015351
    reference: chr 8
allele count: 11
allele frequency: 9.42846367470086e-5
allele num: 116668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-4G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-4G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.616-4G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

8-146015354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015354
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015354
    reference: chr 8
allele count: 4
allele frequency: 3.436012850688062e-5
allele num: 116414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-7C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-7C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.616-7C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

8-146015356-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015356
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015356
    reference: chr 8
allele count: 1
allele frequency: 8.607926178425094e-6
allele num: 116172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-9T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-9T>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31162
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

8-146015364-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015364
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015364
    reference: chr 8
allele count: 1
allele frequency: 8.701402666109778e-6
allele num: 114924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-17T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-17T>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

8-146015366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015366
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015366
    reference: chr 8
allele count: 1
allele frequency: 8.716875871687587e-6
allele num: 114720
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-19C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-19C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

8-146015367-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015367
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015367
    reference: chr 8
allele count: 1
allele frequency: 8.733471904420884e-6
allele num: 114502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-20C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-20C>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18618
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-146015372-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015372
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015372
    reference: chr 8
allele count: 1
allele frequency: 8.808089349258358e-6
allele num: 113532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-25T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-25T>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6675
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7847
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

8-146015378-C-CTCTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015378
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015383
    reference: chr 8
allele count: 1
allele frequency: 8.956400243614087e-6
allele num: 111652
alternate allele: CTCTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-32_616-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-32_*171-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-32_553-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-32_289-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-32_523-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-32_616-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-32_361-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-32_616-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-32_519-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-32_*198-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-32_347-31insAAAGA
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

8-146015383-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015383
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015383
    reference: chr 8
allele count: 2
allele frequency: 1.869438420698422e-5
allele num: 106984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-36G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-36G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-146015387-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015387
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015388
    reference: chr 8
allele count: 11
allele frequency: 1.038951225962447e-4
allele num: 105876
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-41dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-41dupG
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10651
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13261
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-146015390-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015391
    reference: chr 8
allele count: 2635
allele frequency: 2.52563979679862e-2
allele num: 104330
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-44dupG
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-44dupG
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 2.75e1
  variant carriers: 425
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 15358
  bin: 1.75e1
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 2.25e1
  variant carriers: 497
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 7.5e0
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 3.75e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 1.25e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 4.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.25e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.75e1
  variant carriers: 62
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.75e1
  variant carriers: 34
num of homozygotes: 331
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/8-146015390-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015390
    reference: chr 8
allele count: 11
allele frequency: 1.054346784242308e-4
allele num: 104330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-43T>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-43T>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15358
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

8-146015390-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015390
    reference: chr 8
allele count: 1
allele frequency: 9.584970765839164e-6
allele num: 104330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-43T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-43T>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

8-146015390-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015390
    reference: chr 8
allele count: 1
allele frequency: 9.584970765839164e-6
allele num: 104330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-43T>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-43T>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

8-146015395-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015395
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015395
    reference: chr 8
allele count: 2
allele frequency: 2.024127601003967e-5
allele num: 98808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-48G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-48G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7034
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2267
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

8-146015396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015396
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015396
    reference: chr 8
allele count: 1
allele frequency: 1.019596647566223e-5
allele num: 98078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.347-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.519-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.616-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.616-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.616-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*171-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*198-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.361-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.523-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.553-49C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.289-49C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

8-146015694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015694
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015694
    reference: chr 8
allele count: 2
allele frequency: 1.683700099338306e-5
allele num: 118786
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+46C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+46C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15168
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  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: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

8-146015695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015695
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015695
    reference: chr 8
allele count: 3
allele frequency: 2.527252202921504e-5
allele num: 118706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+45G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+45G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7573
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6858
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

8-146015696-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015696
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015696
    reference: chr 8
allele count: 5
allele frequency: 4.2069127991115e-5
allele num: 118852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+44G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+44G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16384
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

8-146015700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015700
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015700
    reference: chr 8
allele count: 3
allele frequency: 2.522534642809095e-5
allele num: 118928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+40C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18920
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

8-146015700-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015700
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015700
    reference: chr 8
allele count: 1
allele frequency: 8.408448809363649e-6
allele num: 118928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+40C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+40C>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18920
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22653
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-146015704-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015704
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015704
    reference: chr 8
allele count: 1
allele frequency: 8.397574780403419e-6
allele num: 119082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+36G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+36G>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-146015713-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015713
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015713
    reference: chr 8
allele count: 1
allele frequency: 8.348499774590506e-6
allele num: 119782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+27G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+27G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3846
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

8-146015717-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015717
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015717
    reference: chr 8
allele count: 3
allele frequency: 2.496338703235255e-5
allele num: 120176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+23G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+23G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

8-146015718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015718
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015718
    reference: chr 8
allele count: 2
allele frequency: 1.6622616732326e-5
allele num: 120318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+22G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+22G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3230
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

8-146015728-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015728
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015728
    reference: chr 8
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+12A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+12A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-146015729-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015729
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015729
    reference: chr 8
allele count: 1
allele frequency: 8.265555775970376e-6
allele num: 120984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+11C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+11C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

8-146015730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015730
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015730
    reference: chr 8
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.552+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+10C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+10C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

8-146015731-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146015731
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146015731
    reference: chr 8
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000534781
  gene symbol: RPL8
  hgvsc: ENST00000534781.1:n.518+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.288+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000529163
  gene symbol: RPL8
  hgvsc: ENST00000529163.1:n.360+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.615+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.*170+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.346+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.*197+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.615+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.522+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.615+9C>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

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

GenotypeQuality
all individuals: 581
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5017
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 825
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.798561151079137e-3
allele num: 556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.137e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

DP
type: SiteQuality
SIO_000300: 4.56857e5

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

QD
type: SiteQuality
SIO_000300: 1.804e1

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

GenotypeQuality
all individuals: 419
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 643
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.129520389843549e-4
allele num: 7798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.413709872073377e-4
allele num: 8286
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 4.57655e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

QD
type: SiteQuality
SIO_000300: 1.358e1

FS
type: SiteQuality
SIO_000300: 1.846e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.299e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.13e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.182033096926714e-4
allele num: 8460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.896e0

DP
type: SiteQuality
SIO_000300: 4.63346e5

MQ
type: SiteQuality
SIO_000300: 5.891e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.391e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.68e-1

QD
type: SiteQuality
SIO_000300: 4.82e0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 10
allele frequency: 5.13874614594039e-3
allele num: 1946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.27942681678608e-4
allele num: 7816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 1.995305164319249e-3
allele num: 8520
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.207e1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.97e-1

MQ
type: SiteQuality
SIO_000300: 5.87e1

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

DP
type: SiteQuality
SIO_000300: 4.65882e5

GenotypeQuality
all individuals: 667
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5039
bin: 9.75e1
variant carriers: 7

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 5.796429399489915e-4
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 1.233045622688039e-3
allele num: 1622
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 4.66413e5

QD
type: SiteQuality
SIO_000300: 1.337e1

MQRankSum
type: SiteQuality
SIO_000300: -2.91e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

FS
type: SiteQuality
SIO_000300: 1.108e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

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

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.833375926399182e-4
allele num: 7826
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.019e0

FS
type: SiteQuality
SIO_000300: 1.3922e1

DP
type: SiteQuality
SIO_000300: 4.66454e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.553e0

VQSLOD
type: SiteQuality
SIO_000300: -2.096e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

GenotypeQuality
all individuals: 884
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1652
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.15233924867481e-4
allele num: 8678
num of homozygotes: 0

Latino
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: 586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2016
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.105e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

FS
type: SiteQuality
SIO_000300: 8.154e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.22e-1

DP
type: SiteQuality
SIO_000300: 4.67094e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.558e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.31e-1

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1654
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 875
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 4.310344827586207e-3
allele num: 232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 70
allele frequency: 4.315659679408138e-2
allele num: 1622
num of homozygotes: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.372369624885636e-3
allele num: 8744
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.887e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

FS
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 5.467e1

QD
type: SiteQuality
SIO_000300: 1.107e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e-1

DP
type: SiteQuality
SIO_000300: 4.70289e5

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003003003003003e-5
allele num: 66600
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.23e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 2.153542e6

QD
type: SiteQuality
SIO_000300: 1.581e1

MQ
type: SiteQuality
SIO_000300: 6.03e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

DP
type: SiteQuality
SIO_000300: 2.154501e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.993e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.422e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e0

FS
type: SiteQuality
SIO_000300: 1.543e0

QD
type: SiteQuality
SIO_000300: 1.401e1

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

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

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

QD
type: SiteQuality
SIO_000300: 1.202e1

FS
type: SiteQuality
SIO_000300: 3.629e0

VQSLOD
type: SiteQuality
SIO_000300: 5.97e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.348e0

DP
type: SiteQuality
SIO_000300: 2.155085e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

FS
type: SiteQuality
SIO_000300: 6.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

DP
type: SiteQuality
SIO_000300: 2.157409e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.715e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.11e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.49e-1

GenotypeQuality
all individuals: 399
bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.000600060006001e-5
allele num: 66660
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 5.85e-1

DP
type: SiteQuality
SIO_000300: 2.157865e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.468e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.299e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.271e1

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

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3686
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3909
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 394
bin: 8.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 26
allele frequency: 2.246414377052013e-3
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 867
allele frequency: 8.342956120092379e-2
allele num: 10392
num of homozygotes: 45

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

Other
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allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.35e-2

FS
type: SiteQuality
SIO_000300: 1.231e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.42e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 2.183242e6

QD
type: SiteQuality
SIO_000300: 1.346e1

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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bin: 7.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.138e0

QD
type: SiteQuality
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FS
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SIO_000300: 0.0e0

MQ
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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SIO_000300: 2.07258e6

VQSLOD
type: SiteQuality
SIO_000300: 8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-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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variant carriers: 5

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

Latino
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allele count: 5
allele frequency: 4.319281271596407e-4
allele num: 11576
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 1.886e0

QD
type: SiteQuality
SIO_000300: 1.513e1

MQRankSum
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SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

DP
type: SiteQuality
SIO_000300: 2.073867e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.75e-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

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

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.77e0

MQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 5.570000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.073742e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

QD
type: SiteQuality
SIO_000300: 1.089e1

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.977e1

DP
type: SiteQuality
SIO_000300: 2.074043e6

MQRankSum
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 1.536e1

FS
type: SiteQuality
SIO_000300: 7.317e0

VQSLOD
type: SiteQuality
SIO_000300: -7.65e-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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.286e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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ClippingRankSum
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QD
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DP
type: SiteQuality
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 1.503237742830712e-3
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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allele frequency: 2.883506343713956e-4
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Other
type: Population
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 6614
num of homozygotes: 0

South Asian
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African
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allele frequency: 1.92270717169775e-4
allele num: 10402
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East Asian
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Latino
type: Population
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Other
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European (Non-Finnish)
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ClippingRankSum
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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BaseQRankSum
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DP
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 10404
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European (Non-Finnish)
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allele frequency: 5.99538355466291e-5
allele num: 66718
num of homozygotes: 0

Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.155802126675913e-4
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: -4.578e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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allele frequency: 4.535833081342606e-4
allele num: 6614
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African
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Other
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East Asian
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ReadPosRankSum
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MQ
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MQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

European (Non-Finnish)
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allele count: 3
allele frequency: 4.496537665997182e-5
allele num: 66718
num of homozygotes: 0

South Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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Other
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African
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East Asian
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QD
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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MQ
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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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GenotypeQuality
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variant carriers: 1

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

East Asian
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num of homozygotes: 0

Other
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African
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allele num: 10406
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European (Finnish)
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 4.077e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

South Asian
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allele num: 16512
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East Asian
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African
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allele frequency: 0.0e0
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Latino
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Other
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

East Asian
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European (Finnish)
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South Asian
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Other
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Latino
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QD
type: SiteQuality
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VQSLOD
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MQ
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DP
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

South Asian
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Latino
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Other
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African
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European (Finnish)
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DP
type: SiteQuality
SIO_000300: 2.070506e6

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.429e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.763e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.991e1

GenotypeQuality
all individuals: 461
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.070363e6

MQRankSum
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SIO_000300: -1.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.384e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 2.59e0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.322e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.148e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.441e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

BaseQRankSum
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SIO_000300: -6.093e0

DP
type: SiteQuality
SIO_000300: 2.068931e6

MQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.08e-1

QD
type: SiteQuality
SIO_000300: 1.214e1

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13965
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.066281e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.108e0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.11e-1

QD
type: SiteQuality
SIO_000300: 2.095e1

GenotypeQuality
all individuals: 3718
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 5.88e-1

DP
type: SiteQuality
SIO_000300: 2.065102e6

MQRankSum
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InbreedingCoeff
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SIO_000300: 3.3e-3

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
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SIO_000300: 4.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.86e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.17e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.516084420660213e-5
allele num: 66524
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.385e0

InbreedingCoeff
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SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
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DP
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QD
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 6.21e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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 frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.222775357809582e-5
allele num: 16070
num of homozygotes: 0

FS
type: SiteQuality
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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variant carriers: 1

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.239081607187422e-5
allele num: 16028
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.91e0

MQRankSum
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FS
type: SiteQuality
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3661
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15838
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.656237929702588e-5
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.909e1

VQSLOD
type: SiteQuality
SIO_000300: -1.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.509e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 2.047252e6

FS
type: SiteQuality
SIO_000300: 2.662e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.563e0

QD
type: SiteQuality
SIO_000300: 1.441e1

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

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3871
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13682
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510710940568632e-5
allele num: 66194
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

FS
type: SiteQuality
SIO_000300: 7.072e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

DP
type: SiteQuality
SIO_000300: 2.03777e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.078e0

QD
type: SiteQuality
SIO_000300: 1.154e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 738
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 157
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 13330
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variant carriers: 0

GenotypeQuality
all individuals: 32225
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.576659038901602e-5
allele num: 65550
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14346
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.344803614876608e-4
allele num: 11508
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.799e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.069e0

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.999261e6

FS
type: SiteQuality
SIO_000300: 8.93e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

GenotypeDepth
all individuals: 121
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variant carriers: 0

GenotypeDepth
all individuals: 190
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3530
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13216
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variant carriers: 0

GenotypeQuality
all individuals: 3777
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variant carriers: 0

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 4127
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532379171902295e-5
allele num: 65258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.65e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 3.616e0

DP
type: SiteQuality
SIO_000300: 1.98358e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.347e0

GenotypeDepth
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4191
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 367
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variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 387
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GenotypeQuality
all individuals: 317
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variant carriers: 0

GenotypeQuality
all individuals: 38
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GenotypeQuality
all individuals: 448
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GenotypeQuality
all individuals: 255
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GenotypeQuality
all individuals: 23
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variant carriers: 1

GenotypeQuality
all individuals: 3776
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variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
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GenotypeQuality
all individuals: 734
bin: 9.75e1
variant carriers: 10

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
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: 856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 8.05978898007034e-4
allele num: 13648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65188
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.981652e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-1

FS
type: SiteQuality
SIO_000300: 1.487e0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

QD
type: SiteQuality
SIO_000300: 1.181e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.442e0

GenotypeDepth
all individuals: 24
bin: 9.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 725
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 31298
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65136
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.484560570071259e-4
allele num: 13472
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.083e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

VQSLOD
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SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.06e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

DP
type: SiteQuality
SIO_000300: 1.976711e6

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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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
all individuals: 23
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GenotypeQuality
all individuals: 458
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.514277126540426e-5
allele num: 13308
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 848
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.497e1

FS
type: SiteQuality
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VQSLOD
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SIO_000300: 2.76e0

BaseQRankSum
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SIO_000300: -8.45e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 3.95e-1

MQRankSum
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SIO_000300: 2.65e-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
all individuals: 718
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1605
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.761811792268645e-5
allele num: 10244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64712
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.745e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.79e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: -6.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.71e0

FS
type: SiteQuality
SIO_000300: 2.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e0

DP
type: SiteQuality
SIO_000300: 1.956565e6

VQSLOD
type: SiteQuality
SIO_000300: -2.16e0

GenotypeQuality
all individuals: 970
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546503355912282e-5
allele num: 64662
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.555e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

DP
type: SiteQuality
SIO_000300: 1.953982e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12274
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.780907668231612e-5
allele num: 10224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.378e0

QD
type: SiteQuality
SIO_000300: 1.404e1

MQ
type: SiteQuality
SIO_000300: 6.09e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.239e0

DP
type: SiteQuality
SIO_000300: 1.951281e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

GenotypeQuality
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bin: 2.5e0
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: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 3691
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171783454417624e-4
allele num: 8534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

FS
type: SiteQuality
SIO_000300: 3.254e0

VQSLOD
type: SiteQuality
SIO_000300: -1.569e0

DP
type: SiteQuality
SIO_000300: 1.926735e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 5.763e1

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

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7012
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GenotypeQuality
all individuals: 11846
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572970082109038e-5
allele num: 63574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.188e0

DP
type: SiteQuality
SIO_000300: 1.847757e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.307e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

QD
type: SiteQuality
SIO_000300: 2.142e1

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
all individuals: 552
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variant carriers: 2

GenotypeQuality
all individuals: 3849
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.235931786557939e-5
allele num: 61806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.22e1

DP
type: SiteQuality
SIO_000300: 1.54814e6

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 4.632e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.091e0

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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bin: 1.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 140
bin: 9.25e1
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.631108501337509e-5
allele num: 61308
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.237317495669389e-3
allele num: 8082
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.805e0

QD
type: SiteQuality
SIO_000300: 3.0e-1

DP
type: SiteQuality
SIO_000300: 1.490413e6

FS
type: SiteQuality
SIO_000300: 3.1437e1

VQSLOD
type: SiteQuality
SIO_000300: -3.381e0

MQRankSum
type: SiteQuality
SIO_000300: -9.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

MQ
type: SiteQuality
SIO_000300: 5.89e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.79e-1

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 49

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1883

GenotypeQuality
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GenotypeQuality
all individuals: 639
bin: 4.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 36

GenotypeQuality
all individuals: 11978
bin: 6.25e1
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GenotypeQuality
all individuals: 418
bin: 4.75e1
variant carriers: 32

Latino
type: Population
allele count: 116
allele frequency: 1.056466302367942e-2
allele num: 10980
num of homozygotes: 2

African
type: Population
allele count: 2433
allele frequency: 2.669519420671495e-1
allele num: 9114
num of homozygotes: 329

South Asian
type: Population
allele count: 9
allele frequency: 9.710832973672853e-4
allele num: 9268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 69
allele frequency: 1.153036328999699e-3
allele num: 59842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 1.084010840108401e-2
allele num: 738
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.852e0

DP
type: SiteQuality
SIO_000300: 1.356229e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-1

QD
type: SiteQuality
SIO_000300: 1.623e1

GenotypeQuality
all individuals: 213
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 639
bin: 4.25e1
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GenotypeQuality
all individuals: 11978
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 4

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.097213078779899e-3
allele num: 9114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.671067143477825e-5
allele num: 59842
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 2.852e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

QD
type: SiteQuality
SIO_000300: 1.623e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 1.356229e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59842
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.207729468599034e-4
allele num: 8280
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

FS
type: SiteQuality
SIO_000300: 2.852e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

QD
type: SiteQuality
SIO_000300: 1.623e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

DP
type: SiteQuality
SIO_000300: 1.356229e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1205
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59842
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.078981441519206e-4
allele num: 9268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9114
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-1

DP
type: SiteQuality
SIO_000300: 1.356229e6

FS
type: SiteQuality
SIO_000300: 2.852e0

QD
type: SiteQuality
SIO_000300: 1.623e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 633
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.531004808909137e-4
allele num: 7902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.3e-1

FS
type: SiteQuality
SIO_000300: 2.071e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.603e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.21e-2

DP
type: SiteQuality
SIO_000300: 1.213461e6

GenotypeQuality
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bin: 4.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.782658300057045e-5
allele num: 56096
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.207911e6

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.763e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.736e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.45e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.81e-1

FS
type: SiteQuality
SIO_000300: 4.698e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

QD
type: SiteQuality
SIO_000300: 4.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.734e0

GenotypeQuality
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variant carriers: 0

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

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: 2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.057542958478566e-5
allele num: 65412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15894
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

BaseQRankSum
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SIO_000300: -2.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.26e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

DP
type: SiteQuality
SIO_000300: 1.639375e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.541912632821724e-4
allele num: 8470
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.644172e6

FS
type: SiteQuality
SIO_000300: 1.045e0

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.72e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.14821810855056e-4
allele num: 15882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65466
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

QD
type: SiteQuality
SIO_000300: 8.109999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

DP
type: SiteQuality
SIO_000300: 1.649892e6

GenotypeQuality
all individuals: 7218
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.881113619262603e-4
allele num: 15948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65476
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.456e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.419e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

FS
type: SiteQuality
SIO_000300: 8.319000000000001e0

DP
type: SiteQuality
SIO_000300: 1.671525e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.36e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 2638
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65476
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.270378730875344e-5
allele num: 15948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.36e-1

FS
type: SiteQuality
SIO_000300: 8.319000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.671525e6

VQSLOD
type: SiteQuality
SIO_000300: -4.456e-1

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.419e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6871
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variant carriers: 1

GenotypeQuality
all individuals: 1849
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.176470588235294e-4
allele num: 8500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65552
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15952
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 1.693376e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.383e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.062e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 1.352e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516484183069971e-5
allele num: 65942
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16070
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.039e1

DP
type: SiteQuality
SIO_000300: 1.738125e6

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.48e-1

FS
type: SiteQuality
SIO_000300: 3.938e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 5.994e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.907540220973057e-4
allele num: 10318
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 2.11e-1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
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SIO_000300: -1.057e0

QD
type: SiteQuality
SIO_000300: 1.271e1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.021513173797438e-5
allele num: 66192
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.441e1

MQRankSum
type: SiteQuality
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503985561738607e-5
allele num: 66490
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.516e0

FS
type: SiteQuality
SIO_000300: 2.059e0

MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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QD
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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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
all individuals: 3282
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1779
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31686
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.308e1

VQSLOD
type: SiteQuality
SIO_000300: -8.481e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

DP
type: SiteQuality
SIO_000300: 1.775427e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.807e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.36e-1

GenotypeQuality
all individuals: 1781
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3946
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3281
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31771
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6893
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8271
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.591e0

VQSLOD
type: SiteQuality
SIO_000300: -3.561e-1

FS
type: SiteQuality
SIO_000300: 3.115e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

QD
type: SiteQuality
SIO_000300: 1.331e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.776236e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.551e0